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

• 89291-76-9 (1S,4R,5S)-(-)-3-<(benzyloxy)methyl>-4,5-O-isopropylidene-2-cyclopenten-1-ol 
• 117307-62-7 (3aR,6aR)-6-Benzyloxymethyl-2,2-dimethyl-4,6a-dihydro-3aH-cyclopenta[d][1,3]dioxol-4-one 
• 5336-08-3 D-Ribono-1,4-lactone 
• 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 
• 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 

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

Stereocontrolled syntheses of 6-epi-trehazolin and 6-epi-trehalamine from D-ribonolactone

6-epi-Trehazolin was synthesized in a stereocontrolled manner, and this synthesis proved that an oxazine structural isomer of 6-epi-trehazolin does not exist.