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37689-19-3

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37689-19-3 Usage

Structure

Contains a five-carbon cyclic ring and a propenyl side chain

Classification

Unsaturated hydrocarbon

Presence of double bond

Yes

Chemical reactions

Can undergo addition and polymerization reactions

Industrial applications

Used as a building block in the synthesis of various organic compounds

Potential applications

Production of flavors, fragrances, and other industrial products

Check Digit Verification of cas no

The CAS Registry Mumber 37689-19-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,7,6,8 and 9 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 37689-19:
(7*3)+(6*7)+(5*6)+(4*8)+(3*9)+(2*1)+(1*9)=163
163 % 10 = 3
So 37689-19-3 is a valid CAS Registry Number.
InChI:InChI=1/C8H12/c1-2-5-8-6-3-4-7-8/h2,6H,1,3-5,7H2

37689-19-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-prop-2-enylcyclopentene

1.2 Other means of identification

Product number -
Other names 1-Allyl-cyclopenten

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:37689-19-3 SDS

37689-19-3Downstream Products

37689-19-3Relevant articles and documents

Conversion of vinyl sulfones to regiospecifically functionalized trisubstituted olefins

Kim, Seong Heon

, p. 4013 - 4014 (2007/10/02)

Conjugate-addition of phenyldimethylsilyllithium (or cuprate) to vinyl sulfones followed by in situ alkylation of the α-sulfonyl anion provides α-alkylated β-silyl sulfones. Treatment of these materials with fluoride provides trisubstituted olefins via th

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