175911-73-6

Basic information

• Product Name: (1-(benzyloxymethyl)cyclopent-3-enyl)methanol
• Synonyms: (1-(benzyloxymethyl)cyclopent-3-enyl)methanol
• CAS NO: 175911-73-6
• Molecular Weight: 218.296
• Mol File: 175911-73-6.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: (1-(benzyloxymethyl)cyclopent-3-enyl)methanol(CAS DataBase Reference)
• NIST Chemistry Reference: (1-(benzyloxymethyl)cyclopent-3-enyl)methanol(175911-73-6)
• EPA Substance Registry System: (1-(benzyloxymethyl)cyclopent-3-enyl)methanol(175911-73-6)

Safety Data

• Hazardous Substances Data: 175911-73-6(Hazardous Substances Data)

Upstream product

• 76910-02-6 3-cyclopenten-1,1-dimethanol 
• 100-39-0 benzyl bromide 
• 100-52-7 benzaldehyde 
• 261510-93-4 8-Phenyl-7,9-dioxaspiro[4.5]dec-2-ene 

Downstream Products

• 261510-99-0 (1α,3α,5α)-3-Benzyloxymethyl-6-oxabicyclo[3.1.0]hexane-3-methanol 
• 1242165-01-0 (1-(benzyloxymethyl)cyclopent-3-enyl)methyl 2,3,4,6-tetra-O-acetyl-β-D-galactopyranoside 
• 1242276-78-3 (1-(benzyloxymethyl)-3,4-dihydroxycyclopentyl)methyl 2,3,4,6-tetra-O-acetyl-β-D-galactopyranoside 
• 1242276-79-4 (3-acetoxy-1-(benzyloxymethyl)-4-hydroxycyclopentyl)methyl 2,3,4,6-tetra-O-acetyl-β-D-galactopyranoside 
• 1242276-81-8 (3-acetoxy-1-O-(4,4'-dimethoxytrityl)methyl-4-hydroxycyclopentyl)methyl 2,3,4,6-tetra-O-acetyl-β-D-galactopyranoside 
• 1242276-82-9 C₄₈H₅₆O₁₉ 
• 544444-28-2 (1R,4R)-4-Benzyloxymethyl-4-hydroxymethylcyclopent-2-en-1-ol 
• 175911-75-8 (1S,4S)-4-Benzyloxymethyl-4-hydroxymethylcyclopent-2-en-1-ol 

Relevant articles and documents

Simple solid-phase synthesis and biological properties of carbohydrate - Oligonucleotide conjugates modified at the 3′-terminus

A novel synthesis method for oligonucleotides possessing a functional moiety at the 3′-terminus was established based on solid-phase synthesis. In order to install the functional group at the 3′-terminus of the oligonucleotide, a solid support possessing

Highly enantioselective rearrangement of quaternary carbon-containing meso-epoxides to allylic alcohols

The asymmetric synthesis of 4-substituted cis-4-(hydroxymethyl)cyclopent-2-en-1-ols 3 (R = alkyl, benzyloxymethyl) via highly enantioselective rearrangement of 3-substituted cis-6-oxabicyclo[3.1.0]hexane-3-methanols 1 (R = alkyl, benzyloxymethyl) is described.