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2-Cyclopentene-1-propanoic acid, also known as 2-cyclopentene-1-carboxylic acid, is a chemical compound with the molecular formula C8H12O2. It is a colorless liquid with a pungent odor and is derived from the cyclopentene ring structure, which is a five-membered ring with one double bond. This organic acid is a key intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals. It is used in the production of fragrances, flavorings, and other industrial applications. The compound is characterized by its unique reactivity due to the presence of both a cycloalkene and a carboxylic acid functional group, which allows for a range of chemical transformations and reactions.

2910-57-8

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2910-57-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2910-57-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,9,1 and 0 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 2910-57:
(6*2)+(5*9)+(4*1)+(3*0)+(2*5)+(1*7)=78
78 % 10 = 8
So 2910-57-8 is a valid CAS Registry Number.

2910-57-8SDS

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-(cyclopent-2-enyl)-propionic acid

1.2 Other means of identification

Product number -
Other names 3-Cyclopent-2-enyl-propionsaeure

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:2910-57-8 SDS

2910-57-8Relevant academic research and scientific papers

Black-light-induced radical/ionic hydroxymethylation of alkyl iodides with atmospheric co in the presence of tetrabutylammonium borohydride

Kobayashi, Shoji,Kawamoto, Takuji,Uehara, Shohei,Fukuyama, Takahide,Ryu, Ilhyong

supporting information; experimental part, p. 1548 - 1551 (2010/07/06)

(Figure Presented) Tin-free radical/ionic hydroxymethylation of secondary and tertiary alkyl iodides proceeded efficiently in the presence of tetrabutylammonium borohydride as the hydrogen source under atmospheric pressure of CO In conjunction with photoirradiation using black light. Two possible mechanisms were proposed, both of which involve hybrid radical/ionic processes.

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