344294-32-2

Basic information

• Product Name: Cyclopentanecarboxylic acid, 3-formyl-, methyl ester (9CI)
• Synonyms: Cyclopentanecarboxylic acid, 3-formyl-, methyl ester (9CI);FORMYL-CYCLOPENTANECARBOXYLIC ACID METHYL ESTER;3-FORMYL-CYCLOPENTANECARBOXYLIC ACID METHYL ESTER
• CAS NO: 344294-32-2
• Molecular Formula: C₈H₁₂O₃
• Molecular Weight: 156.17908
• Product Categories: ALDEHYDE;CARBOXYLICESTER
• Mol File: 344294-32-2.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• CAS DataBase Reference: Cyclopentanecarboxylic acid, 3-formyl-, methyl ester (9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: Cyclopentanecarboxylic acid, 3-formyl-, methyl ester (9CI)(344294-32-2)
• EPA Substance Registry System: Cyclopentanecarboxylic acid, 3-formyl-, methyl ester (9CI)(344294-32-2)

Safety Data

• Hazardous Substances Data: 344294-32-2(Hazardous Substances Data)

Upstream product

• 58240-93-0 (+)-cis-(1R,3S)-3-hydroxymethyl-1-carbomethoxycyclopentane 
• 84545-00-6 3-(methoxycarbonyl)-cyclopentane-1-carboxylic acid 
• 2435-36-1 cyclopentane?1,3?dimethyl formate 
• 498-66-8 norborn-2-ene 
• 108-24-7 acetic anhydride 
• 17190-90-8 2-methoxybicyclo<2.2.1>hept-2-ene 

Downstream Products

• 139585-47-0 ((E)-3-Propenyl)-cyclopentanecarboxylic acid 
• 139585-45-8 phenyl<3-(1-propenyl)cyclopent-1-yl>methanone 

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

NEW CHEMISTRY OF ZWITTERIONIC PEROXIDES ARISING BY PHOTOOXYGENATION OF ENOL ETHERS

The rose bengal-sensitized photooxygenation of 2-methoxynorborn-2-ene (1) in acetaldehyde gave cis-1-carboxaldehyde-3-carbomethoxycyclopentane (31percent) and the cis and trans-Me derivatives of the cis-fused exo-1,2,4-trioxanes arising by addition of a molecule of oxygen and acetaldehyde to 1 at C3 and C2 respectively (13percent).Similar photooxygenation of 2-(methoxymetylidene)adamantane in the presence of acetaldehyde, propionaldehyde and pivalaldehyde gave adamantanone (31-42percent), and the cis and trans tricyclo3.7>decane-2-spiro-6'- in yields of 32-53percent.Trioxane formation under similar conditions was experienced for 1,1-di-t-butyl-2-methoxyethene and 2-(methylmercaptomethylidene)adamantane.The results are discussed in terms of an intermediate zwitterionic peroxide which can either close directly to a 1,2-dioxetane or, if aldehyde is present, condense across the CO function giving the 1,2,4-trioxane.