58240-93-0

Basic information

• Product Name: METHYL CIS-3-HYDROXYMETHYLCYCLOPENTANE-1-CARBOXYLATE
• Synonyms: METHYL CIS-3-HYDROXYMETHYLCYCLOPENTANE-1-CARBOXYLATE;rel-methyl (1R,3S)-3-(hydroxymethyl)cyclopentane-1-carboxylate
• CAS NO: 58240-93-0
• Molecular Formula: C8H14O3
• Molecular Weight: 158.19
• Mol File: 58240-93-0.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 230°C at 760 mmHg
• Flash Point: 91.5°C
• Appearance: /
• Density: 1.091g/cm³
• Vapor Pressure: 0.0129mmHg at 25°C
• Refractive Index: 1.467
• CAS DataBase Reference: METHYL CIS-3-HYDROXYMETHYLCYCLOPENTANE-1-CARBOXYLATE(CAS DataBase Reference)
• NIST Chemistry Reference: METHYL CIS-3-HYDROXYMETHYLCYCLOPENTANE-1-CARBOXYLATE(58240-93-0)
• EPA Substance Registry System: METHYL CIS-3-HYDROXYMETHYLCYCLOPENTANE-1-CARBOXYLATE(58240-93-0)

Safety Data

• Hazardous Substances Data: 58240-93-0(Hazardous Substances Data)

Usage

InChI:InChI=1/C8H14O3/c1-11-8(10)7-3-2-6(4-7)5-9/h6-7,9H,2-5H2,1H3/t6-,7+/m0/s1

Upstream product

• 2435-36-1 cyclopentane?1,3?dimethyl formate 
• 84545-00-6 3-(methoxycarbonyl)-cyclopentane-1-carboxylic acid 
• 541-41-3 chloroformic acid ethyl ester 
• 96443-42-4 (+)-cis-(1S,3R)-3-carbomethoxycyclopentane carboxylic acid 

Downstream Products

• 344294-32-2 methyl 3-formylcyclopentane-1-carboxylate 

Relevant articles and documents

Pharmacophore-Based Design of Phenyl-[hydroxycyclohexyl] Cycloalkyl-Carboxamide Mitofusin Activators with Improved Neuronal Activity

Mitochondrial fragmentation from defective fusion or unopposed fission contributes to many neurodegenerative diseases. Small molecule mitofusin activators reverse mitochondrial fragmentation in vitro, promising a novel therapeutic approach. The first-in-c

Enzymes in organic synthesis. 33. Stereoselective pig liver esterase-catalyzed hydrolyses of meso cyclopentyl-, tetrahydrofuranyl-, and tetrahydrothiophenyl-1,3-diesters

Preparative-scale pig liver esterase-catalyzed hydrolyses of five-membered ring meso-1,3-diesters are enantiotopically selective.While pro-S enantiotopic selectivity is exhibited in each case, the absolute configuration sense of the hydrolysis in the cyclopentyl series is opposite to that of both the tetrahydrofuranyl and tetrahydrothiophenyl diesters.The enantiomeric excess levels induced are in the 34-46percent range.