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344294-32-2

Cyclopentanecarboxylic acid, 3-formyl-, methyl ester (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 344294-32-2 Structure

  • Basic information

    1. Product Name: Cyclopentanecarboxylic acid, 3-formyl-, methyl ester (9CI)
    2. Synonyms: Cyclopentanecarboxylic acid, 3-formyl-, methyl ester (9CI);FORMYL-CYCLOPENTANECARBOXYLIC ACID METHYL ESTER;3-FORMYL-CYCLOPENTANECARBOXYLIC ACID METHYL ESTER
    3. CAS NO:344294-32-2
    4. Molecular Formula: C8H12O3
    5. Molecular Weight: 156.17908
    6. EINECS: N/A
    7. Product Categories: ALDEHYDE;CARBOXYLICESTER
    8. Mol File: 344294-32-2.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: Cyclopentanecarboxylic acid, 3-formyl-, methyl ester (9CI)(CAS DataBase Reference)
    10. NIST Chemistry Reference: Cyclopentanecarboxylic acid, 3-formyl-, methyl ester (9CI)(344294-32-2)
    11. EPA Substance Registry System: Cyclopentanecarboxylic acid, 3-formyl-, methyl ester (9CI)(344294-32-2)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 344294-32-2(Hazardous Substances Data)

344294-32-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 344294-32-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,4,4,2,9 and 4 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 344294-32:
(8*3)+(7*4)+(6*4)+(5*2)+(4*9)+(3*4)+(2*3)+(1*2)=142
142 % 10 = 2
So 344294-32-2 is a valid CAS Registry Number.

344294-32-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-Formyl-cyclopentanecarboxylic acid methyl ester

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:344294-32-2 SDS

344294-32-2Relevant articles and documents

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

Bernstein, Peter R.,Dang, Xiawei,Devanathan, Sriram,Dorn, Gerald W.,Franco, Antonietta,Fu, Lijun,Walters, Daniel,Williams, Sidney B.

, p. 12506 - 12524 (2021/09/11)

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

Oxidative Cyclization of δ,ε- and ε,ζ-Unsaturated Enol Silyl Ethers and Unsaturated Siloxycyclopropanes

Snider, Barry B.,Kwon, Taesoo

, p. 2399 - 2410 (2007/10/02)

Oxidative cyclization of δ,ε- and ε,ζ-unsaturated enol silyl ethers 4a and 4b with cupric triflate and cuprous oxide or ceric ammonium nitrate and sodium bicarbonate in acetonitrile provides the tricyclic ketones 5a and 5b stereoselectively.These cyclizat

NEW CHEMISTRY OF ZWITTERIONIC PEROXIDES ARISING BY PHOTOOXYGENATION OF ENOL ETHERS

Jefford, Charles W.,Boukouvalas, John,Kohmoto, Shigeo,Bernardinelli, Gerald

, p. 2081 - 2088 (2007/10/02)

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.

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