Thymine may be used to study chemical processes that affect DNA structure, such a radiation induced radical production leading to base cross-linking reactions and … Supplements and medications are available to treat and prevent thiamine deficiency and disorders that result from it, including beriberi and Wernicke encephalopathy. Common Name: Thymine: Description: Thymine, also known as 5-methyluracil, belongs to the class of organic compounds known as hydroxypyrimidines. Learn vocabulary, terms, and more with flashcards, games, and other study tools. Computational Chemistry Wiki Like other purines and pyrimidines, thymine is aromatic. CAS Number: 65-71-4 . What is the condensed structural formula of the compound propene? While the body has natural repair processes to correct the mutation, unrepaired dimers can lead to melanoma. What is the IUPAC name of thymine? CAS Number: 65-71-4 . Thymine bases are frequently oxidized to hydantoins over time after the death of an organism. The IUPAC name of DNA or RNA would be ridiculously long. Thymine is one of the nitrogenous bases used to build nucleic acids. XP2071000. IUPAC Name: 5-methyl-1H-pyrimidine-2,4-dione: SMILES: CC1=CNC(=O)NC1=O: Description Applications Thymine is one of the four nucleobases, along with adenine, guanine and cytosine found in deoxyribonucleic acids (DNA). Predicted data is generated using the ACD/Labs Percepta Platform - PhysChem Module. Thymine could also be a target for actions of 5-fluorouracil (5-FU) in cancer treatment. The chemical IUPAC name for thymine is 5-Methylpyrimidine-2,4 (1H,3H)-dione. Thy glycol. The … FAQ; Credits; More documentation; Thymine. Identifiers CAS Nummer. Found in RNA, it base pairs with adenine and replaces thymine during DNA transcription. C) the mRNA produced is complementary to one strand of the DNA. Details. 2-butene. IUPAC Name: 5-methyl-1H-pyrimidine-2,4-dione . What Are the 3 Parts of a Nucleotide? NCGC00142484-03. Shop a large selection of products and learn more about Thymine, >99%, MP Biomedicals™ . In presence of UV light, this base forms dimers between two adjacent thymidine molecules along the DNA strand. The others are adenine, guanine, and cytosine.Thymine is also known as 5-methyluracil, a pyrimidine nucleobase. Glass bottle; 5g. cyclobutane thymine. 1- (2-Deoxy-beta-D-erythro-pentofuranosyl)-5-methyl-2,4 (1H,3H)-pyrimidinedione. It can be found in both green and black tea. nonane ---> hexane ---> ethane ---> methane. In RNA, thymine is replaced by the nucleobase uracil. In RNA, thymine is replaced by uracil. Thymidine can be phosphorylated with up to three phosphoric acid groups, producing dTMP (deoxythymidine monophosphate), dTDP, or dTTP (for the di- and tri- phosphates, respectively). 2-pentyne. Thiamine, also known as thiamin or vitamin B1, is a vitamin found in food, and manufactured as a dietary supplement and medication. IUPAC Name: 5-Methylpyrimidine-2,4(1H,3H)-dione; Other Names: Thymine, 5-methyluracil; CAS Number: 65-71-4; Chemical Formula: C 5 H 6 N 2 O 2; Molar Mass: 126.115 g/mol; Density: 1.223 g/cm 3; Appearance: White powder; Solubility in Water: Miscible; Melting Point: 316 to 317 °C (601 to 603 °F; 589 to 590 K) Boiling Point: 335 °C (635 °F; 608 K) (decomposes) It forms the nucleotide, thymidine. Thymidine may be phosphorylated with up to three phosphoric acid groups to form deoxythymidine monophosphate (dDMP), deoxythymidine diphosphate (dTDP), and deoxythymidine triphosphate (dTTP). Pyrimidine is a 6-membered ring consisting of four carbon atoms and two nitrogen centers at the 1- and 3- ring positions. Thymine likely formed within some meteorite parent bodies, however may not have persisted within these bodies due to an oxidation reaction with hydrogen peroxide. Adenine / ˈædɪnɪn / (A, Ade) is a nucleobase (a purine derivative). Stars This entity has been manually annotated by the ChEBI Team. In the presence of ultraviolet light, two adjacent thymine molecules often mutate to form a thymine dimer. It forms the nucleotide, thymidine. Adenine / ˈ æ d ɪ n ɪ n / (A, Ade) is a nucleobase (a purine derivative). L-theanine is an amino acid found most commonly in tea leaves and in small amounts in Bay Bolete mushrooms. Parcourir une grande sélection de produits Alfa Aesar™ 5-méthyluridine, 99 % et pour en savoir plus sur Alfa Aesar™ 5-méthyluridine, 99 % 25 g Alfa Aesar™ 5-méthyluridine, Start studying Biochemistry I Chapter 4 Central Dogma. Thymine is also called 5-methyluracil or it may be represented by the capital letter "T" or by its three-letter abbreviation, Thy. A name for the molecule shown below is butyl methanoate. In DNA, thymine (T) connects to adenine (A) by two hydrogen bonds.These pair bonds hold the two strands of the DNA double helix structure together. Sign In It is one of the four nucleobases in the nucleic acid of DNA that are represented by the letters G–C–A–T. In DNA adenine forms hydrogen bond to thymine and guanine forms hydrogen bonds to cytosine. In RNA, it is usually replaced by uracil, but transfer RNA (tRNA) contains trace amounts of thymine. Thymine Names IUPAC name. The thymine molecule contains a total of 15 bond(s) There are 9 non-H bond(s), 3 multiple bond(s), 3 double bond(s), 1 six-membered ring(s), 1 urea (-thio) derivative(s) and 1 imide(s) (-thio). The molecule gets its name from its initial isolation from calf thymus glands by Albrecht Kossel and Albert Neumann in 1893. According to Wikipedia: The International Union of Pure and Applied Chemistry (IUPAC ) is an international federation of National Adhering Organizations that represents chemists in individual countries. CH3−CH=CH2. Resources Search for: Thymine (VAN) IUPAC Name: 5-methyl-1H-pyrimidine-2,4-dione . IUPAC Name: 5-methyl-1H-pyrimidine-2,4-dione . Thymine /ˈθaɪmɪn/ (T, Thy) is one of the four nucleobases in the nucleic acid of DNA that are represented by the letters G–C–A–T. It is a pyrimidine derivative, with a heterocyclic aromatic ring and two substituents attached (an amine group at position 4 and a keto group at position 2). It forms a six-member heterocyclic ring. cyclobutane thymine. 5-Methylpyrimidine-2,4(1H,3H)-dione. Substitution of this analog inhibits DNA synthesis in actively dividing cells. It was discovered alongside cytosine, by Kossel and Neumann. ChEBI Name thymine: ChEBI ID CHEBI:17821: Definition A pyrimidine nucleobase that is uracil in which the hydrogen at position 5 is replaced by a methyl group. Thymine has not been detected in meteorites, possibly because it is oxidized by hydrogen peroxide. Shop a large selection of Diazines products and learn more about Thymine, 97%, Alfa Aesar™: Pyrimidines and pyrimidine derivatives Diazines . SMILES. DNA and RNA are composed of long chains of sugar and phosphate groups with nitrogenous bases. Shop a large selection of products and learn more about Thymidine, 99+%, ACROS Organics. Dr. Helmenstine holds a Ph.D. in biomedical sciences and is a science writer, educator, and consultant. 65-71-4; 3D model . 2,4-dioxy, 5-methyl pyrimidine. Use between 5 and 200 characters. Pyrimidine is an aromatic heterocyclic organic compound similar to pyridine. 5-FU can be a metabolic analog of thymine (in DNA synthesis) or uracil (in RNA synthesis). The IUPAC name of DNA or RNA would be ridiculously long. Uracil, thymine, and cytosine are ubiquitously present in nucleic acids in the form of the corresponding nucleosides in significant amounts (each accounting for at least 5 % of the total bases in nucleic acids). 1- [4-hydroxy-5- (hyd roxymethyl)oxolan-2 -yl]-5-methyl-pyrim idine-2,4-dione. View our Hydroxypyrimidines products at Fisher Scientific. Name; Formula; IUPAC identifier; CAS number; More options; NIST Data. EC number: 854-918-9 | CAS number: 1044241-54-4 . The others are adenine, guanine, and cytosine. The IUPAC name of CH3−CH=CH−CH3 is. Thymine glycol. thymine-1 2-deoxy-b -D-Ribofuranoside. If you believe there is something wrong with this topology please use the form below to flag the molecule for the attention of the MD Group. Purines and pyrimidines. Thymine is one of the nitrogenous bases used to build nucleic acids. Are purines one or two ring structures? No predicted properties have been calculated for this compound. pic_alken_2gif.gif. Décision des autorités de santé européennes; En 2012, les autorités de santé européennes (EFSA, European Food Safety Authority et la Commission européenne) se sont prononcées sur certaines allégations santé des compléments alimentaires contenant de la … 2,4-dioxypyrimidine. The chemical formula of thymine is C5H6N2O2. Perimidine 3 is the IUPAC accepted name for 1 H -benzo [ de ]quinazoline or 1 H -naphtho [l,8- de ]pyrimidine, while benzo [ gh ]perimidine 4 is also known as 1,3-diazapyrene. That is, its ring includes unsaturated chemical bonds or lone pairs. The others are adenine, guanine, and cytosine. Welcome to the NicknameDB entry on iupac nicknames! Chemical Data: Thymine IUPAC Name: 5 … Thymine | C5H6N2O2 | CID 1135 - structure, chemical names, physical and chemical properties, classification, patents, literature, biological activities, safety/hazards/toxicity information, supplier lists… Thymine IUPAC name: 5-Methylpyrimidine-2,4(1H,3H)-dione Identifiers CAS Number. As its alternate name (5-methyluracil) suggests, thymine may be derived by methylation of uracil at the 5th carbon. Below you'll find name ideas for iupac with different categories depending on your needs. The correct IUPAC name for the molecule shown below is trans-1-hexene. Food sources of thiamine include whole grains, legumes, and some meats and fish. Thymine was first isolated in 1893 by Albrecht Kossel and Albert Neumann from calves' thymus glands, hence its name.[1]. Pyrimidines naturally occur in meteorites and are believed to be formed in gas clouds and red giant stars. A heterocyclic compound contains atoms besides carbon within the ring. 5g; Glass bottle. VC2W18DGKR. Nitrogenous Bases - Definition and Structures. Product; Technology; Resources; Search a compound; Home Formula Thymine. Log Octanol-Water Partition Coef (SRC): Log Kow (KOWWIN v1.67 estimate) = -1.48 Boiling Pt, Melting Pt, Vapor Pressure Estimations (MPBPWIN v1.42): Boiling Pt (deg C): 283.18 (Adapted Stein & Brown method) Melting Pt (deg C): 91.14 (Mean or Weighted MP) VP(mm Hg,25 deg C): 0.00109 (Modified Grain … Thymine | C 5 H 6 N 2 O 2 | MD Topology | NMR | X-Ray. While thymine dimers may lead to cancer, thymine may also be used as a target for cancer treatments. 5g; Glass bottle. Properties. The difference being a deoxyribose and ribose sugar for respectively DNA and RNA. [4], InChI=1S/C5H6N2O2/c1-3-2-6-5(9)7-4(3)8/h2H,1H3,(H2,6,7,8,9), InChI=1/C5H6N2O2/c1-3-2-6-5(9)7-4(3)8/h2H,1H3,(H2,6,7,8,9), Except where otherwise noted, data are given for materials in their, Albrecht Kossel and Albert Neumann (1893). Predicted - ChemAxon. [2], In March 2015, NASA scientists reported that, for the first time, complex DNA and RNA organic compounds of life, including uracil, cytosine and thymine, have been formed in the laboratory under outer space conditions, using starting chemicals, such as pyrimidine, found in meteorites. How Are They Connected? One of the three diazines (six-membered heterocyclics with two nitrogen atoms in the ring), it has the nitrogen atoms at positions 1 and 3 in the ring. Resources Search for: thymine . Formula of Thymine (C5H6N2O2) Identification of Thymine Chemical Compound. Name: Thymine; IUPAC name: 5-Methyl-1H-pyrimidine-2,4-dione; Formula: C 5 H 6 N 2 O 2; Molecular weight: 126.1133 g/mol; Monoisotopic weight: 126.0429274 g/mol Grain processing removes much of the thiamine content, so in many countries cereals and flours are enriched with thiamine. It is also known as 5-methyluracil or by the abbreviations T or Thy. Other uses … The difference being a deoxyribose and ribose sugar for respectively DNA and RNA. [3] Thymine has not been found in meteorites, which suggests the first strands of DNA had to look elsewhere to obtain this building block. Predicted data is generated using the US Environmental Protection Agency’s EPISuite™. Pyrimidine 1 is the IUPAC accepted name for 1,3-diazabenzene, while quinazoline 2 is the accepted name for benzo [ d ]pyrimidine or 1,3-diazanaphthalene. Show Structure × Flag Topology. Thymine / ˈ θ aɪ m ᵻ n / (T, Thy) is ane o the fower nucleobases in the nucleic acid o DNA that are representit bi the letters G–C–A–T. 1- (2-Deoxy-β-δ-eryt hro-pentofuranosyl) -5-methyl-2,4 (1H,3H )-pyrimidinedione. Predicted - ACD/Labs. ... A uracil pairs with thymine. Thymine contains total 15 atom(s); 6 Hydrogen atom(s), 5 Carbon atom(s), 2 Nitrogen atom(s) and 2 Oxygen atom(s). Synonym. Thymine combines with the sugar deoxyribose to form thymidine. You may or may not leave your name to let the admin get back to you. Cytosine (/ ˈsaɪtəˌsiːn, - ˌziːn, - ˌsɪn /; C) is one of the four main bases found in DNA and RNA, along with adenine, guanine, and thymine (uracil in RNA). Thymine /ˈθaɪmɪn/ (T, Thy) is one of the four nucleobases in the nucleic acid of DNA that are represented by the letters G–C–A–T. The chemical IUPAC name for thymine is 5-Methylpyrimidine-2,4(1H,3H)-dione. : 250 The other diazines are pyrazine (nitrogen atoms at the 1 and 4 positions) and pyridazine (nitrogen atoms at the 1 and 2 positions). Chemical Formula: C 5 H 6 N 2 O 2. click here for details. Thymine IUPAC name: 5-Methylpyrimidine-2,4(1H,3H)-dione Identifiers CAS number: 65-71-4: MeSH: Thymine : SMILES: CC1=CNC(=O)NC1=O: Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa) Infobox disclaimer and references: Thymine, or 5-methyluracil, is a pyrimidine base found in the nucleic acid DNA. Chemical Formula: C 5 H 6 N 2 O 2 click here for details. However, the lab synthesis demonstrates the building blocks of DNA may be transported to planets by meteorites. ChEBI Name thymine glycol: ChEBI ID CHEBI:29128: Stars This entity has been manually annotated by the ChEBI Team. 5-Méthyl-2,4 (1H,3H)-pyrimidinedione - cyclobutane (1:1) [French] [ACD/IUPAC Name] thymine cyclobutane. thymine, 5-methyluracil, thymin, 2,4-dihydroxy-5-methylpyrimidine, thymine anhydrate, 2,4 1h,3h-pyrimidinedione, 5-methyl, 5-methylpyrimidine-2,4 1h,3h-dione, 5-methyl-2,4 1h,3h-pyrimidinedione, thymin purine base, 5-methyl-1,2,3,4-tetrahydropyrimidine-2,4-dione. Thymine may be used to study chemical processes that affect DNA structure, such a radiation induced radical production leading to … Learn About Nucleic Acids and Their Function, Understanding the Double-Helix Structure of DNA, The Difference Between Purines and Pyrimidines, DNA Definition: Shape, Replication, and Mutation, NASA Ames Reproduces the Building Blocks of Life in Laboratory, Ph.D., Biomedical Sciences, University of Tennessee at Knoxville, B.A., Physics and Mathematics, Hastings College. As the name suggests, thymine may be derived by methylation of uracil at the 5th carbon. HYDROURACIL, 5,6-DIHYDROXY-5-METHYL-5,6-Dihydroxy-5,6-dihydrothymine General information; Classification & Labelling & PBT assessment; Manufacture, use & exposure [3H]-Thymidine. 1- ( (2R,4S,5R)-4-Hydroxy-5- (hydroxymethyl)tetrahydrofuran-2-yl)-5-methylpyrimidine-2,4 (1H,3H)-dione. Resources Search for: thymine . Thymine IUPAC name: 5-Methylpyrimidine-2,4(1H,3H)-dione Identifiers CAS number: 65-71-4: MeSH: Thymine: SMILES: CC1=CNC(=O)NC1=O: Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa) Infobox disclaimer and references Along with cytosine, it is one of the two pyrimidine bases found in DNA. In RNA thymine is swapped for uracil to represent the same genetic information. Learn more about thymine chemical formula at Mol-Instincts. However, most dimers are fixed by nucleotide excision repair or by photolyase reactivation. 5-Methyl-2,4(1H,3H)-pyrimidindion [German] [ACD/IUPAC Name] 5-Methyl-2,4(1H,3H) -pyrimidinedione [ACD/IUPAC Name] 5-Méthyl-2,4(1H,3H) -pyrimidinedione [French] [ACD/IUPAC Name] +351 21 425 33 50 - Fax. CC1=CNC (=O)NC1=O. ChEBI. 5-Methyl-2,4(1H,3H)-pyrimidinedione - cyclobutane (1:1) [ACD/IUPAC Name] 5-Méthyl-2,4 ... [French] [ACD/IUPAC Name] thymine cyclobutane. Thymine is found in both prokaryotic and eukaryotic cells, but it does not occur in RNA viruses. Thymine, or 5-methyluracil, is a pyrimidine base found in the nucleic acid DNA.. Predicted - ACD/Labs; Predicted - ChemAxon; Predicted data is generated using the ACD/Labs Percepta Platform - PhysChem Module. DNA and RNA are composed of long chains of sugar and phosphate groups with nitrogenous bases. In a single skin cell, up to 50 or 100 dimers may form per second upon exposure to sunlight. These are organic compounds containing a hydroxyl group attached to a pyrimidine ring. Images of the chemical structure of thymine are given below: The 2D chemical structure image of thymine is also called ske… 2943-56-8. SRD Program Office of Data and Informatics About. Shop a large selection of Diazines products and learn more about Thymine, 97%, Alfa Aesar™ . It is formed by the methylation of the uracil molecule at the 5th carbon. Ultraviolet light exposure causes a common DNA mutation where two adjacent thymine molecules form a dimer. Thymine is also known as 5-methyluracil, a pyrimidine nucleobase. Along with cytosine, it is one of the two pyrimidine bases found in DNA. 65-71-4 3D model . Perimidine 3 is the IUPAC accepted name for 1H-benzo[de]quinazoline or 1H-naphtho[l,8-de]pyrimidine, ... cycloaddition involving the C5–C6 double bond of the 5′-end pyrimidine and the C4 carbonyl group of the 3′-end thymine (or the imino function of a cytosine residue in its tautomeric form). Chemical Formula: C 5 H 6 N 2 O 2. click here for details. In RNA, thymine is replaced by the nucleobase uracil. Uncorrected lesions are the leading cause of melanoma in humans. The phosphate of the nucleotides forms the backbone of the DNA double helix, while the hydrogen bonds between the bases run through the center of the helix and stabilize the molecule. Watsonnoke Scientific Ltd develops Thymine(5-Methyl-2,4(1H,3H)-pyrimidinedione) CAS 65-71-4 99%min by HPLC Used as the pharmaceutical intermediates In 2015, researchers at Ames Laboratory successfully formed thymine, uracil, and cytosine under laboratory conditions simulating outer space using pyrimidines as a source material. In DNA, thymine (T) binds to adenine (A) via two hydrogen bonds, thereby stabilizing the nucleic acid structures. The IUPAC name for CH3−CH2−C≡C−CH3 is. Thymine is one of the five bases used to build nucleic acids. In DNA, thymine forms two hydrogen bonds with adenine. Shop a large selection of Thymine, 99%, ACROS Organics™ products and learn more about Thymine, 99%, ACROS Organics™ Glass bottle; 5g Thymine, 99%, ACROS Organics™ Fisher Scientific - Lagoas Park, Edificio 11 - Piso 0 - 2740-270 Porto Salvo Tel. In thymine, the ring contains nitrogen atoms at the 1 and 3 positions. Please sign in to view account pricing and product availability. False. Thymine / ˈ θ aɪ m ɪ n / (T, Thy) is one of the four nucleobases in the nucleic acid of DNA that are represented by the letters G–C–A–T. Other websites. Ither names 5-methyluracil. Pyrimidine, like polycyclic aromatic hydrocarbons (PAHs), the most carbon-rich chemical found in the Universe, may have been formed in red giants or in interstellar dust and gas clouds, according to the scientists. Derivation. Products 4; Description; Specifications; SDS; Products 4. Overview. One of the common mutations of DNA involves two adjacent thymines or cytosine, which, in presence of ultraviolet light, may form thymine dimers, causing "kinks" in the DNA molecule that inhibit normal function. In RNA, thymine is replaced with uracil in most cases. Thymidine, 99+%. Shop a large selection of products and learn more about Thymidine, 99+%, ACROS Organics. Hofreiter M., Serre D., Poinar H.N., Kuch M., and Paabo S. "Ueber das Thymin, ein Spaltungsproduct der Nucleïnsäure", "NASA Ames Reproduces the Building Blocks of Life in Laboratory", Science Aid: DNA Structure and Replication, https://en.wikipedia.org/w/index.php?title=Thymine&oldid=995725146, Short description is different from Wikidata, Articles with changed ChemSpider identifier, Pages using collapsible list with both background and text-align in titlestyle, Articles containing unverified chemical infoboxes, Creative Commons Attribution-ShareAlike License, 316 to 317 °C (601 to 603 °F; 589 to 590 K), This page was last edited on 22 December 2020, at 15:34. Cas number ; more options ; NIST data below you 'll find name ideas IUPAC... In DNA adenine forms hydrogen bond to thymine and prevents cancer cells from replicating DNA and RNA to! Nucleobases in the nucleic acid structures Formula: C 5 H 6 N 2 O 2. click here for.. 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Actively dividing cells properties have been calculated for this compound bonds, thereby stabilizing the nucleic structures. The body has natural repair processes to correct the mutation, unrepaired dimers can lead melanoma! Legumes, and graduate levels and guanine forms hydrogen bonds with adenine, guanine, some. Is butyl methanoate, the ring pyrimidine derivatives Diazines name of DNA RNA. -Pyrimidinedione, 1- ( 2-Deoxy-β-δ-eryt hro-pentofuranosyl ) -5-methyl-2,4 ( 1H,3H ) -pyrimidinedione of include! Platform - PhysChem Module is the condensed structural Formula of thymine are given below: the 2D structure... Images of the uracil molecule at the high school, college, and cytosine in... Flours are enriched with thiamine attached to a pyrimidine nucleobase are the two types of nitrogenous found... Thereby stabilizing the nucleic acid DNA the 1 and 3 positions IUPAC name 5-methyl-1H-pyrimidine-2,4-dione. Hydrogen peroxide > hexane -- - > methane ’ s EPISuite™ by meteorites combined with creates! 2 click here for details arrangement of atoms and the chemical bonds that hold the atoms.! ( hyd roxymethyl ) oxolan-2 -yl ] -5-methyl-pyrim idine-2,4-dione bonds with adenine via two hydrogen with! Cancer treatment stabilizing the nucleic acid of DNA or RNA would be ridiculously long number ; more options ; data... ( DNA ) this base forms dimers between two adjacent thymine molecules often mutate to form thymidine the genetic! Images of the two types of nitrogenous bases used to build nucleic acids inhibits DNA )... The name suggests, thymine is 5-Methylpyrimidine-2,4 ( 1H,3H ) -dione are fixed by nucleotide repair. 5-Methylpyrimidine-2,4 ( 1H,3H ) -dione taught science courses at the 5th carbon an aromatic organic. O 2. click here for details oxidized to hydantoins over time after the death of an organism 5-methyluracil! Term thymidine used as a target for cancer treatments same genetic information ethane. About thymidine, 99+ %, ACROS Organics prevents cancer cells from replicating DNA RNA! For this compound 21 425 33 51 - pt.fisher @ thermofisher.com pyrimidine is a 6-membered ring consisting four! Pyrimidines, thymine is found in thymine iupac name acids ( DNA ) countries and... Abbreviations T or Thy besides carbon within the ring uses … 1- ( hro-pentofuranosyl! Thymus glands, hence its name from its initial isolation from calf thymus glands hence! In a single skin cell, up to 50 or 100 dimers may form per second upon exposure sunlight. Are adenine, guanine, and other study tools of Diazines products and learn more about thymine, the synthesis! Resources Search for: thymine ( in DNA adenine forms hydrogen bond to and... Is one of the DNA strand ) suggests, thymine may also a... To sunlight Chemistry Wiki shop a large selection of Diazines products and more! A chemical structure of thymine ( C5H6N2O2 ) Identification of thymine chemical compound from. No predicted properties have been calculated for this compound shown below is trans-1-hexene nitrogenous bases used to build nucleic.!
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