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1,2-Butadiene, 4-chloro-3-methyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

76397-24-5

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76397-24-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 76397-24-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,3,9 and 7 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 76397-24:
(7*7)+(6*6)+(5*3)+(4*9)+(3*7)+(2*2)+(1*4)=165
165 % 10 = 5
So 76397-24-5 is a valid CAS Registry Number.

76397-24-5SDS

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-chloro-3-methylbuta-1,2-diene

1.2 Other means of identification

Product number -
Other names 1,2-Butadiene,4-chloro-3-methyl

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:76397-24-5 SDS

76397-24-5Upstream product

76397-24-5Relevant academic research and scientific papers

Reactions of 3-Chloro-3-methyl-1-butyne with Hydrogen Chloride: Evidence Against an Electrophilic Addition Reaction

Stammann, Guenter,Rehman, Zillur,Griesbaum, Karl

, p. 3103 - 3111 (2007/10/02)

Reactions of 3-chloro-3-methyl-1-butyne (1) with an excess of anhydrous hydrogen chloride in the liquid phase afforded approx. 16 products.Major product was 1,1,3-trichloro-3-methylbutane (6).In addition, (E)-1,3-dichloro-3-methyl-1-butene (5) and (Z)- and (E)-1,3-dichloro-2-methyl-2-butene (11a, b) were formed in considerable amounts.The expected products of an electrophilic addition to the triple bond, however, were only found in very minute amounts.The formation of the products obtained was rationalized by heterolysis of the C-Cl bond in the substrate 1 and subsequent reactions of the ensuing intermediate mesomeric cation A.

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