143191-83-7

Basic information

• Product Name: 4(S)-(3,4-dihydro-2,4-dioxo-5-methyl-1(2H)-pyrimidinyl)tetrahydro-2(S)-furanmethanol
• Synonyms: 4(S)-(3,4-dihydro-2,4-dioxo-5-methyl-1(2H)-pyrimidinyl)tetrahydro-2(S)-furanmethanol
• CAS NO: 143191-83-7
• Molecular Formula: C10H14N2O4
• Molecular Weight: 226
• Mol File: 143191-83-7.mol
• Article Data: 5

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 4(S)-(3,4-dihydro-2,4-dioxo-5-methyl-1(2H)-pyrimidinyl)tetrahydro-2(S)-furanmethanol(CAS DataBase Reference)
• NIST Chemistry Reference: 4(S)-(3,4-dihydro-2,4-dioxo-5-methyl-1(2H)-pyrimidinyl)tetrahydro-2(S)-furanmethanol(143191-83-7)
• EPA Substance Registry System: 4(S)-(3,4-dihydro-2,4-dioxo-5-methyl-1(2H)-pyrimidinyl)tetrahydro-2(S)-furanmethanol(143191-83-7)

Safety Data

• Hazardous Substances Data: 143191-83-7(Hazardous Substances Data)

Upstream product

• 151223-91-5 4(S)-<3,4-dihydro-2,4-dioxo-5-methyl-1(2H)-pyrimidinyl>tetrahydro-2(S)-furanmethanol benzoate 
• 20881-04-3 1,2:3,5-di-O-isopropylidene-D-xylofuranose 
• 6022-96-4 5-O-benzoyl-α-D-xylofuranose 
• 143191-76-8 1,4-anhydro-5-O-benzoyl-3-deoxy-2-O-p-toluenesulfonyl-D-ribitol 
• 65-71-4 thymin 
• 151825-71-7 Toluene-4-sulfonic acid (3S,4R,5R)-4-benzyloxy-5-benzyloxymethyl-tetrahydro-furan-3-yl ester 
• 138679-69-3 1,4-anhydro-3,5-di-O-benzyl-D-ribitol 
• 55775-39-8 1-O-methyl-3,5-di-O-benzyl-D-ribofuranoside 
• 55735-86-9 3,5-O-dibenzyloxy-1,2-O-isorpopylidene-α-D-ribofuranose 
• 143191-74-6 methyl 5-O-benzoyl-3-deoxy-D-erythro-pentofuranose 
• 143191-75-7 2(S)-(O-benzoylmethyl)tetrahydrofuran-4(R)-ol 
• 20031-21-4 1,2-O-isopropylidene-α-D-xylose 
• 4105-29-7 [(3aR,5S,6aR)-2,2-dimethyltetrahydrofuro[2,3-d][1,3]dioxol-5-yl]methyl benzoate 
• 532-20-7 D-xylofuranose 

Relevant articles and documents

Synthesis of purine and pyrimidine isodideoxynucleosides from (S)- glycydol using iodoetherification as key step. Synthesis of (S,S)-iso-ddA

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Synthesis of Conceptually New, Potentially Anti-viral, Low-Toxity, Acid- and Enzyme-stable Furanoid and Pyranoid Nucleosides

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Synthesis and anti-HIV activity of isonucleosides

A series of isomeric 2',3'-dideoxynucleosides which contains a modified carbohydrate moiety has been prepared. This class of compounds was designed to mimic the activity of known anti-HIV dideoxynucleosides, while imparting enhanced chemical and enzymatic