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38108-82-6

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38108-82-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 38108-82-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,1,0 and 8 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 38108-82:
(7*3)+(6*8)+(5*1)+(4*0)+(3*8)+(2*8)+(1*2)=116
116 % 10 = 6
So 38108-82-6 is a valid CAS Registry Number.

38108-82-6SDS

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 2,3-bis(bromomethyl)-1,4-dimethylbenzene

1.2 Other means of identification

Product number -
Other names 2,3-Bis-brommethyl-1,4-dimethyl-benzol

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:38108-82-6 SDS

38108-82-6Relevant articles and documents

Mechanism-Inspired Design of Bifunctional Catalysts for the Alternating Ring-Opening Copolymerization of Epoxides and Cyclic Anhydrides

Abel, Brooks A.,Lidston, Claire A. L.,Coates, Geoffrey W.

, p. 12760 - 12769 (2019/08/26)

Advances in catalysis have enabled the ring-opening copolymerization of epoxides and cyclic anhydrides to afford structurally and functionally diverse polyesters with controlled molecular weights and dispersities. However, the most common systems employ b

Synthesis and crystal structures of 1,4,8,11-Tetraalkyl-6,13- diphenylpentacenes

Kitamura, Chitoshi,Naito, Takao,Yoneda, Akio,Kawase, Takeshi,Komatsu, Toshiki

, p. 771 - 773 (2011/01/08)

Two 1,4,8,11-tetraalkyl-6,13-diphenylpentacenes were prepared. X-ray analysis revealed that the methyl derivative had a herringbone arrangement with π-overlap, while the propyl derivative had a slipped-parallel structure without π-overlap. The solid-state

AN IMPROVED METHOD FOR THE PREPARATION OF o-QUINODIMETHANES

Rubottom, G. M.,Wey, J. E.

, p. 507 - 514 (2007/10/02)

The use of zinc-silver couple for preparation of the o-qionodimethane from 3,6-dimethyl-1,2-bis(bromomethyl)benzene, 1, is described.

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