127682-77-3

Basic information

• Product Name: 2(R)-<(dimethoxy)methyl>-4(S)-tetrahydrofuran
• Synonyms: 2(R)-<(dimethoxy)methyl>-4(S)-tetrahydrofuran
• CAS NO: 127682-77-3
• Molecular Weight: 316.375
• Mol File: 127682-77-3.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 2(R)-<(dimethoxy)methyl>-4(S)-tetrahydrofuran(CAS DataBase Reference)
• NIST Chemistry Reference: 2(R)-<(dimethoxy)methyl>-4(S)-tetrahydrofuran(127682-77-3)
• EPA Substance Registry System: 2(R)-<(dimethoxy)methyl>-4(S)-tetrahydrofuran(127682-77-3)

Safety Data

• Hazardous Substances Data: 127682-77-3(Hazardous Substances Data)

Upstream product

• 3396-71-2 3-deoxy-1,2-O-isopropylidene-α-D-ribofuranose 
• 3396-72-3 3-deoxy-1,2-O-(1-methylethylidene)-α-D-erythro-pentofuranose 4-methylbenzenesufonate 
• 127682-76-2 (3R,5S)-5-Dimethoxymethyl-tetrahydro-furan-3-ol 
• 98-59-9 p-toluenesulfonyl chloride 
• 6022-96-4 5-O-benzoyl-α-D-xylofuranose 
• 20881-04-3 1,2:3,5-di-O-isopropylidene-D-xylofuranose 
• 20031-21-4 1,2-O-isopropylidene-α-D-xylose 
• 532-20-7 D-xylofuranose 
• 127682-76-2 (2R,4S)-4-hydroxy-2-dimethoxymethyltetrahydrofuran 

Downstream Products

• 127682-82-0 (2R-cis)-4-(6-chloro-9H-purin-9-yl)-tetrahydro-2-furanmethanol 
• 127682-78-4 (2R-trans)-tetrahydro-4-[[(4-methylphenyl)-sulfonyl]oxy]-2-furanmethanol 
• 127682-80-8 (2R-cis)-4-aminotetrahydro-2-furanmethanol 
• 127682-82-0 (2R-cis)-4-(6-chloro-9H-purin-9-yl)tetrahydrofuran-2-methanol 
• 127682-78-4 (2R-trans)-tetrahydro-4-<<(4-methylphenyl)sulfonyl>oxy>-2-furanmethanol 
• 127682-80-8 (2R-cis)-4-aminotetrahydro-2-furanmethanol 
• 127682-75-1 IsoddA 

Relevant articles and documents

New isomeric analogues of anti-HIV active azidonucleosides

Synthesis and antiviral studies of novel 2'-isomeric dideoxynucleosides of the D-related class are described. The target compounds are analogues of anti-HIV active 4'-azido-2'-deoxynucleosides.

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