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81216-95-7

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81216-95-7 Usage

General Description

2-Bromo-1-(3-bromo-2-thienyl)-1-ethanone is an organic chemical compound with the molecular formula C6H4Br2OS. It is a bromo-thienyl-ethanone derivative, which contains a bromine atom attached to a thiophene ring and an ethanone group. 2-BROMO-1-(3-BROMO-2-THIENYL)-1-ETHANONE is commonly used as a building block in organic synthesis and pharmaceutical research. It is a highly reactive compound and has potential applications in the development of new drugs, agrochemicals, and materials. Its chemical structure and properties make it useful for the preparation of various functionalized molecules. Additionally, it is important to handle this chemical with caution, as it may pose health hazards if not used properly.

Check Digit Verification of cas no

The CAS Registry Mumber 81216-95-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,1,2,1 and 6 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 81216-95:
(7*8)+(6*1)+(5*2)+(4*1)+(3*6)+(2*9)+(1*5)=117
117 % 10 = 7
So 81216-95-7 is a valid CAS Registry Number.
InChI:InChI=1/C6H4Br2OS/c7-3-5(9)6-4(8)1-2-10-6/h1-2H,3H2

81216-95-7SDS

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 2-bromo-1-(3-bromothiophen-2-yl)ethanone

1.2 Other means of identification

Product number -
Other names bromobromothienylethanone

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:81216-95-7 SDS

81216-95-7Relevant articles and documents

Direction of 3-bromothiophene acylation with succinyl chloride

Smirnov,Afanas'Ev,Prostakishin,Belen'Kii

, p. 386 - 391 (2013)

In the reaction of 3-bromothiophene with succinyl chloride in the presence of AlCl3, a mixture of three isomeric dibromo-substituted 1,4-di(2-thienyl)butane-1,4-diones was formed. The main component was the unsymmetrical 1-(3-bromo-2-thienyl)-4-(4-bromo-2-thienyl)butane-1,4-dione rather than 1,4-di-(3-bromo-2-thienyl)butane-1,4-dione expected according to the orientation rules.

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