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3-Cyclohexene-1-butanoic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

13487-63-3

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13487-63-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 13487-63-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,4,8 and 7 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 13487-63:
(7*1)+(6*3)+(5*4)+(4*8)+(3*7)+(2*6)+(1*3)=113
113 % 10 = 3
So 13487-63-3 is a valid CAS Registry Number.

13487-63-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-cyclohex-3-en-1-ylbutanoic acid

1.2 Other means of identification

Product number -
Other names 3-Cyclohexene-1-butanoic 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:13487-63-3 SDS

13487-63-3Relevant academic research and scientific papers

Direct Synthesis of Carboxylic Acids from Organoboranes

Hara, Shoji,Kishimura, Kotaro,Suzuki, Akira,Dhillon, Ranjit S.

, p. 6356 - 6360 (2007/10/02)

Direct Synthesis of carboxylic acids through a two carbon atom homologation from organoboranes has been achieved, by the reaction with the dianion of phenoxyacetic acid.It is now possible to synthesize alkanoic, alkenoic, or alkynoic acids, from the corresponding alkenes, dienes, or enynes, respectively, via hydroboration.The reaction is tolerant of various functional groups present in alkenes, thus giving the corresponding carboxylic acids with chloro, sulfide, ether, acetal, and thioacetal functionalities in good yields.

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