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67546-50-3

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67546-50-3 Usage

General Description

(E)-1-chloro-3-bromo-1-propene, also known as bromochloropropene, is a chemical compound with the formula C3H4ClBr. It is a colorless liquid with a pungent odor and is primarily used as an intermediate for the synthesis of various chemicals, including pharmaceuticals, pesticides, and other organic compounds. It is known to be a reactive and potentially hazardous compound, and should be handled with caution. Its chemical structure consists of a propene backbone with chlorine and bromine substituents, making it a useful building block for the production of a variety of different organic materials.

Check Digit Verification of cas no

The CAS Registry Mumber 67546-50-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,7,5,4 and 6 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 67546-50:
(7*6)+(6*7)+(5*5)+(4*4)+(3*6)+(2*5)+(1*0)=153
153 % 10 = 3
So 67546-50-3 is a valid CAS Registry Number.

67546-50-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name E-3-bromo-1-chloropropene

1.2 Other means of identification

Product number -
Other names (E)-1-CHLORO-3-BROMO-1-PROPENE

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:67546-50-3 SDS

67546-50-3Relevant articles and documents

PROCESS FOR THE PREPARATION OF OPTICALLY ACTIVE (4E)-5- HALO-2-ALKYLPENT-4-ENOIC ACIDS AND THEIR ESTER DERIVATIVES

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Page/Page column 27, (2008/06/13)

A process for the preparation of optically active (4E)-5-halo-2-alkylpent-4-enoic acids and their ester derivatives by a stereoselective synthesis which employs camphorsultam as chiral auxiliary is disclosed; in particular methyl (2S, 4E)-5-chloro-2-isopropylpent-4-enoate is prepared, which is a key intermediate in the manufacturing of the new anti-hypertension drug Aliskiren. Furthermore novel N-(5-halo-2-alkylpent-4-enoyl) camphorsultams are provided. A process for the hydrolysis of substituted N-acylcamphorsultams with strong acids is also provided.

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