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57846-06-7

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57846-06-7 Usage

Molecular structure

A thiophene ring with two bromine atoms at the 2 and 5 positions and a dibromomethyl group at the 3 position.

Reactivity

Highly reactive due to the presence of bromine atoms and the thiophene ring, making it suitable for the synthesis of various organic molecules and as a building block for more complex chemical structures.

Toxicity

Highly toxic, posing potential risks to human health and the environment.

Applications

Potential uses in the pharmaceutical and agrochemical industries.

Handling and storage

Requires careful handling and storage to minimize risks due to its toxicity and reactivity.

Check Digit Verification of cas no

The CAS Registry Mumber 57846-06-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,8,4 and 6 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 57846-06:
(7*5)+(6*7)+(5*8)+(4*4)+(3*6)+(2*0)+(1*6)=157
157 % 10 = 7
So 57846-06-7 is a valid CAS Registry Number.
InChI:InChI=1/C5H2Br4S/c6-3-1-2(4(7)8)5(9)10-3/h1,4H

57846-06-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,5-dibromo-3-(dibromomethyl)thiophene

1.2 Other means of identification

Product number -
Other names 2,5-dibromo-3-dibromomethylthiophene

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:57846-06-7 SDS

57846-06-7Relevant articles and documents

RING BROMINATION IN THE ATTEMPTED NITRATION OF 2,5-DIBROMO-3-DIBROMOMETHYLTHIOPHEN

Coyle, John D.,Haws, Edmund J.,Oduntan, Olufemi,Rogers, John T.

, p. 1175 - 1178 (2007/10/02)

Treatment of 2,5-dibromo-3-dibromomethylthiophen with mixed nitric and sulphuric acids or with fuming (>96percent) nitric acid gives 2,4,5-tribromothiphen-3-carbaldehyde after aqueous work-up.

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