113890-37-2

Basic information

• Product Name: (4R,5S)-tetrahydro-2H-pyran-2,4,5-triol
• CAS NO: 113890-37-2
• Molecular Weight: 134.132
• Mol File: 113890-37-2.mol
• Article Data: 20

Chemical Properties

• CAS DataBase Reference: (4R,5S)-tetrahydro-2H-pyran-2,4,5-triol(CAS DataBase Reference)
• NIST Chemistry Reference: (4R,5S)-tetrahydro-2H-pyran-2,4,5-triol(113890-37-2)
• EPA Substance Registry System: (4R,5S)-tetrahydro-2H-pyran-2,4,5-triol(113890-37-2)

Safety Data

• Hazardous Substances Data: 113890-37-2(Hazardous Substances Data)

Upstream product

• 190186-36-8 (2R,3S)-5-(Phenyl-hydrazono)-pentane-1,2,3-triol 
• 17434-50-3 9-(2-Deoxy-alpha-D-erythro-pentopyranosyl)-adenine 
• 1032468-38-4 anilide of 2-deoxy-L-ribose 
• 64429-68-1 methyl 3,4-O-isopropylidene-2-deoxy-β-L-arabinopyranoside 
• 6960-39-0 methyl 3,4-O-isopropylidene-β-L-arabinopyranoside 
• 91-09-8 methyl β-L-arabinopyranoside 
• 1373340-79-4 methyl 3,4-O-isopropylidene-2-O-phenoxythiocarbonyl-β-L-arabinopyranoside 
• 1032153-57-3 1-t-butyl-2-deoxy-L-ribopyranose 
• 152202-52-3 L-arabinal 
• 817621-87-7 2-deoxy-4,5-O-isopropylidene-L-ribose ethylene acetal 
• 817622-79-0 1-O-methyl-2-deoxy-3,4-O-isopropylidene-L-glucopyranoside 
• 288069-41-0 (2S,4R,5S)-(-)-4-allyl-5-hydroxy-2-phenyl-1,3-dioxane 
• 432492-83-6 benzyl 3,4-O-isopropylidene-2-O-[N-phenylthioxocarbamoyl]-β-L-arabinopyranoside 
• 432492-84-7 benzyl 3,4-O-isopropylidene-2-O-[1-imidazolyl(thiocarbonyl)]-β-L-arabinopyranoside 

Downstream Products

• 110509-24-5 2,3-Dideoxy-3-(3,4,5,6-tetrabromophthalimido)-β-D-threo-pentopyranose 
• 110472-45-2 2,3-Dideoxy-3-(3,4,5,6-tetrabromophthalimido)-α-D-threo-pentopyranose 
• 110472-56-5 2,3-Dideoxy-3-(3,4,5,6-tetrabromophthalimido)-5-O-(triphenylmethyl)-α-D-erythro-pentofuranose 
• 110472-57-6 2,3-Dideoxy-3-(3,4,5,6-tetrabromophthalimido)-5-O-(triphenylmethyl)-β-D-erythro-pentofuranose 
• 73958-00-6 (5S,6S)-epoxy-10-formyl-(7E,9E)-decadienoic acid methyl ester 
• 104091-31-8 (2R,4R,5S)-4-(2-Methyl-6-phenylamino-purin-9-yl)-tetrahydro-pyran-2,5-diol 
• 104091-21-6 (2S,4R,5S)-4-(2-Methyl-6-phenylamino-purin-9-yl)-tetrahydro-pyran-2,5-diol 
• 104091-35-2 (2R,4R,5S)-4-[6-(4-Butyl-phenylamino)-2-methyl-purin-9-yl]-tetrahydro-pyran-2,5-diol 
• 104091-25-0 (2S,4R,5S)-4-[6-(4-Butyl-phenylamino)-2-methyl-purin-9-yl]-tetrahydro-pyran-2,5-diol 
• 104091-34-1 (2R,4R,5S)-4-[6-(4-Isopropyl-phenylamino)-2-methyl-purin-9-yl]-tetrahydro-pyran-2,5-diol 
• 104091-24-9 (2S,4R,5S)-4-[6-(4-Isopropyl-phenylamino)-2-methyl-purin-9-yl]-tetrahydro-pyran-2,5-diol 
• 104091-33-0 (2R,4R,5S)-4-[6-(4-Ethyl-phenylamino)-2-methyl-purin-9-yl]-tetrahydro-pyran-2,5-diol 
• 104091-23-8 (2S,4R,5S)-4-[6-(4-Ethyl-phenylamino)-2-methyl-purin-9-yl]-tetrahydro-pyran-2,5-diol 
• 104091-36-3 (2R,4R,5S)-4-[6-(4-Chloro-phenylamino)-2-methyl-purin-9-yl]-tetrahydro-pyran-2,5-diol 

Relevant articles and documents

Structure-based rationalization of aldolase-catalyzed asymmetric synthesis

This paper describes a structure-based approach to elucidate the stereospecificity, including inversion of enantioselectivity, of the 2-deoxyribose-5-phosphate aldolase-catalyzed asymmetric aldol addition reaction using unnatural substrates designed for t

Improved and practical synthesis of 2-deoxy-l-ribose by hypophosphite-mediated deoxygenation

An improved and practical route for a large-scale synthesis of 2-deoxy-L-ribose starting from L-arabinose has been developed. This is the first reported synthesis of 2-deoxy-L-ribose in which deoxygenation has been mediated by hypophosphite reagents instead of by organotin reagents.

A new synthetic strategy for 2-deoxy-D-ribose via palladium(II)-catalyzed cyclization of aldehyde

We achieved a total synthesis of 2-deoxy-D-ribose through intramolecular Pd(II)-catalyzed cyclization of aldehyde via an unstable hemiacetal intermediate as a key step. The Japan Institute of Heterocyclic Chemistry.