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6425-67-8

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6425-67-8 Usage

General Description

1,2-dibromo-4,5-bis(bromomethyl)benzene is a chemical compound with the molecular formula C8H6Br4. It is a type of aromatic compound that contains two bromine atoms attached to the 1 and 2 positions, as well as two bromomethyl groups attached to the 4 and 5 positions of the benzene ring. 1,2-dibromo-4,5-bis(bromomethyl)benzene is commonly used as a building block in organic synthesis and can be used to create a variety of other chemical compounds. It is important to handle this compound with care, as it is classified as a hazardous substance and may cause skin and eye irritation, as well as respiratory and digestive issues if it is inhaled or ingested.

Check Digit Verification of cas no

The CAS Registry Mumber 6425-67-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,4,2 and 5 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 6425-67:
(6*6)+(5*4)+(4*2)+(3*5)+(2*6)+(1*7)=98
98 % 10 = 8
So 6425-67-8 is a valid CAS Registry Number.

6425-67-8SDS

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 1,2-dibromo-4,5-bis(bromomethyl)benzene

1.2 Other means of identification

Product number -
Other names 1,2-dibromo-4,5-bis-bromomethyl-benzene

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:6425-67-8 SDS

6425-67-8Relevant articles and documents

Discotic Mesophases Obtained from Substituted Metallophthalocyanines. Toward Liquid Crystalline One-Dimensional Conductors

Piechocki, Christian,Simon, Jacques,Skoulios, Antoine,Guillon, Daniel,Weber, Patrick

, p. 5245 - 5247 (1982)

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Benzoladderene Mechanophores: Synthesis, Polymerization, and Mechanochemical Transformation

Yang, Jinghui,Horst, Matias,Romaniuk, Joseph A. H.,Jin, Zexin,Cegelski, Lynette,Xia, Yan

, p. 6479 - 6483 (2019)

We have previously reported a polymechanophore system, polyladderene, which underwent dramatic bond rearrangement in response to mechanical force to yield semiconducting polyacetylene. Herein, we report the scalable synthesis of benzoladderenes as new mec

2,3-Dihalo- and 2,3,6,7-Tetrahaloanthracenes by Vollhardt Trimerization

Hoffmann, Hendrik,Mukanov, Diana,Ganschow, Michael,Rominger, Frank,Freudenberg, Jan,Bunz, Uwe H. F.

, p. 9826 - 9834 (2019/08/20)

We efficiently synthesized otherwise difficult to obtain 2,3- and 2,3,6,7-halogenated anthracenes with diverse east/west substituents. Key steps involve the (i) Vollhardt cyclization of bis(propargyl)benzenes with bis(trimethylsilyl)acetylene, (ii) halo-desilylation introducing chlorine, bromine, or iodine substituents, and (iii) dehydrogenation. Pd catalysis allows selective functionalization at the anthracenes' east/west positions. A tetrahydropentacene is synthesized and derivatized via the same strategy, employing tetrapropargylbenzene.

A new and simple synthetic approach to functionalized sulphone derivatives by the Suzuki-Miyaura cross-coupling reaction

Kotha, Sambasivarao,Ghosh, Arun Kumar

, p. 227 - 231 (2007/10/03)

Synthesis of various highly functionalized sulphone derivatives are reported via the bis Suzuki-Miyaura (SM) cross-coupling reaction as a key step. In this regard, the dibromo sulphone 8, prepared from the corresponding sultine derivative 7 by thermal rea

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