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108384-36-7

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108384-36-7 Usage

General Description

1-Cyclopentene-1-carboxylic acid, 3-oxo- (9CI) is a chemical compound with the molecular formula C6H8O3. It is a cyclic carboxylic acid with a ketone functional group. This chemical is a colorless liquid with a fruity odor and is used in the production of pharmaceuticals and as a building block in organic synthesis. It is also known for its potential use in the development of new materials and as a reagent in chemical reactions. Although further research is needed to fully understand its properties and potential applications, 1-Cyclopentene-1-carboxylic acid, 3-oxo- (9CI) shows promise as a versatile and valuable compound in the chemical industry.

Check Digit Verification of cas no

The CAS Registry Mumber 108384-36-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,8,3,8 and 4 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 108384-36:
(8*1)+(7*0)+(6*8)+(5*3)+(4*8)+(3*4)+(2*3)+(1*6)=127
127 % 10 = 7
So 108384-36-7 is a valid CAS Registry Number.
InChI:InChI=1/C6H6O3/c7-5-2-1-4(3-5)6(8)9/h3H,1-2H2,(H,8,9)

108384-36-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-oxocyclopent-1-enecarboxylic acid

1.2 Other means of identification

Product number -
Other names 3-oxocyclopent-1-ene-1-carboxylic acid

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:108384-36-7 SDS

108384-36-7Relevant articles and documents

All-carbon quaternary stereogenic centers by enantioselective Cu-catalyzed conjugate additions promoted by a chiral N-heterocyclic carbene

Brown, M. Kevin,May, Tricia L.,Baxter, Carl A.,Hoveyda, Amir H.

, p. 1097 - 1100 (2008/03/15)

(Chemical Equation Presented) Necessity is the mother of invention: When the available catalysts do not cut it, a new one has to be developed. A chiral N-heterocyclic carbene (NHC) is used in the first catalytic asymmetric conjugate addition of alkyl- and

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