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6214-28-4

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6214-28-4 Usage

General Description

"(2E)-3-chlorobut-2-enoic acid" is a chemical compound with the molecular formula C4H5ClO2. It is an unsaturated carboxylic acid, with a double bond between the second and third carbon atoms in the carbon chain. The presence of a chlorine atom in the molecule gives it its characteristic properties. This chemical is used in the synthesis of other organic compounds and can also be used as a reagent in chemical reactions. It is important to handle this compound with caution, as it may pose health risks if not used properly.

Check Digit Verification of cas no

The CAS Registry Mumber 6214-28-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,2,1 and 4 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 6214-28:
(6*6)+(5*2)+(4*1)+(3*4)+(2*2)+(1*8)=74
74 % 10 = 4
So 6214-28-4 is a valid CAS Registry Number.

6214-28-4SDS

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 (E)-3-chlorobut-2-enoic acid

1.2 Other means of identification

Product number -
Other names 3-chloroisocrotonic 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:6214-28-4 SDS

6214-28-4Relevant articles and documents

Hydrochlorination of 2,3-acetylenic acids with thionyl chloride in dimethylformamide

Urdaneta, Neudo A.,Herrera, Julio C.,Salazar, Jose,Lopez, Simon E.

, p. 3003 - 3009 (2007/10/03)

The reaction of 2,3-acetylenic acids (1a-d) with thionyl chloride in DMF under mild conditions gave E,Z-3-chloro-2-alkenoic acids (2a-d) or esters (3a-d) depending on treating the reaction mixture with either water or alcohols.

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