160343-91-9

Basic information

• Product Name: <1R-(1α,2α,3α,4α,5α)>-1-<(Benzyloxy)methyl>-2,3-(isopropylidenedioxy)-6-oxabicyclo<3.1.0>hexan-4-ol
• Synonyms: <1R-(1α,2α,3α,4α,5α)>-1-<(Benzyloxy)methyl>-2,3-(isopropylidenedioxy)-6-oxabicyclo<3.1.0>hexan-4-ol
• CAS NO: 160343-91-9
• Molecular Weight: 292.332
• Mol File: 160343-91-9.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: <1R-(1α,2α,3α,4α,5α)>-1-<(Benzyloxy)methyl>-2,3-(isopropylidenedioxy)-6-oxabicyclo<3.1.0>hexan-4-ol(CAS DataBase Reference)
• NIST Chemistry Reference: <1R-(1α,2α,3α,4α,5α)>-1-<(Benzyloxy)methyl>-2,3-(isopropylidenedioxy)-6-oxabicyclo<3.1.0>hexan-4-ol(160343-91-9)
• EPA Substance Registry System: <1R-(1α,2α,3α,4α,5α)>-1-<(Benzyloxy)methyl>-2,3-(isopropylidenedioxy)-6-oxabicyclo<3.1.0>hexan-4-ol(160343-91-9)

Safety Data

• Hazardous Substances Data: 160343-91-9(Hazardous Substances Data)

Upstream product

• 5336-08-3 D-Ribono-1,4-lactone 
• 117307-62-7 (3aR,6aR)-6-Benzyloxymethyl-2,2-dimethyl-4,6a-dihydro-3aH-cyclopenta[d][1,3]dioxol-4-one 
• 89291-76-9 (1S,4R,5S)-(-)-3-<(benzyloxy)methyl>-4,5-O-isopropylidene-2-cyclopenten-1-ol 
• 160343-90-8 <1R-(1α,2α,3α,4α,5α)>-1-<(Benzyloxy)methyl>-2,3-(isopropylidenedioxy)-4-<(4-methoxybenzyl)oxy>-6-oxabicyclo<3.1.0>hexane 
• 160531-14-6 3,4-O-Isopropylidene-aldehydo-L-ribo-penturono-5,2-lactone 
• 160343-89-5 <1S-(1α,4α,5α)>-3-<(Benzyloxy)methyl>-4,5-(isopropylidenedioxy)-1-<(4-methoxybenzyl)oxy>-2-cyclopentene 
• 160343-87-3 <1S-(1α,4α,5α)>-3-<<(tert-Butyldimethylsilyl)oxy>methyl>-4,5-(isopropylidenedioxy)-1-<(4-methoxybenzyl)oxy>-2-cyclopentene 
• 160343-88-4 <1S-(1α,4α,5α)>-3-(Hydroxymethyl)-4,5-(isopropylidenedioxy)-1-<(4-methoxybenzyl)oxy>-2-cyclopentene 
• 160343-77-1 (Z)-5-O-(tert-Butyldimethylsilyl)-4,5-didehydro-2,3-O-isopropylidene-D-erythro-penturono-1,4-lactone 
• 160343-78-2 (3aR,6aR)-6-{{[(1,1-dimethylethyl)dimethylsilyl]oxy}methyl}-3a,6a-dihydro-2,2-dimethyl-4H-cyclopenta[d]-1,3-dioxol-4-one 
• 160343-79-3 (3aS,4S,6aR)-6-{{[(1,1-dimethylethyl)dimethylsilyl]oxy}methyl}-3a,6a-dihydro-2,2-dimethyl-4H-cyclopenta[d]-1,3-dioxol-4-ol 
• 100-39-0 benzyl bromide 
• 30725-00-9 2,3-O-isopropylidene-D-ribonic-γ-lactone 

Downstream Products

• 160343-93-1 <1R-(1α,2β,3β,4β,5β)>-5-Amino-1-<(benzyloxy)methyl>-2,3-(isopropylidenedioxy)-1,4-cyclopentanediol 
• 160343-94-2 <1R-(1α,2β,3β,4β,5β)>-<1-<(Benzyloxy)methyl>-1,2,3,4-tetrahydroxycyclopentane-5-yl>amino (2,3,4,5-tetra-O-benzyl-1-deoxy-α-D-glucopyranos-1-yl)amino thioketone 
• 160343-95-3 <3aR-(3aα,4α,5β,6β,6aα)>-4-<(Benzyloxy)methyl>-2-<(2,3,4,6-tetra-O-benzyl-1-deoxy-α-D-glucopyranos-1-yl)-amino>-3a,5,6,6a-tetrahydro-4H-cyclopentoxazole-4,5,6-triol 
• 160344-09-2 <3aR-(3aα,4α,5β,6β,6aα)>-4-<(Benzyloxy)methyl>-2-(benzylamino)-3a,5,6,6aα-tetrahydro-4H-cyclopentoxazole-4,5,6-triol 
• 160344-08-1 <1R-(1α,2β,3β,4β,5β)>-<1-<(Benzyloxy)methyl>-1,2,3,4-tetrahydroxycyclopent-5-yl>amino benzylamino thioketone 
• 160343-92-0 <1R-(1α,2β,3β,4β,5β)>-5-Azido-1-<(benzyloxy)methyl>-2,3-(isopropylidenedioxy)-1,4-cyclopentanediol 

Relevant articles and documents

Chiral pool synthesis of 4a-substituted carbocyclic cyclopentanoid nucleoside precursors, I

A suitable protected D-ribono-1,4-lactone derivative has been used for the straightforward chiral pool synthesis of cyclopentanoid nucleoside precursors. Thus, epoxidation followed by deoxygenation or regioselective ring opening led to nucleoside precurso

Synthesis of 6-epi-trehazolin from D-ribonolactone: Evidence for the non-existence of a 5,6-ringfused structural isomer of 6-epi-trehazolin

6-Epi-trehazolin was synthesized in a stereocontrolled manner, and this synthesis provided proof for the non-existence of oxazine structural isomer of 6-epi-trehazolin.