Welcome to LookChem.com Sign In|Join Free
  • or
Benzene, 2,3-bis(bromomethyl)-1,4-dimethyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

38108-82-6

Post Buying Request

38108-82-6 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

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 academic research and scientific papers

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.

supporting information, 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

A 1, 2, 3, 4 - four-toluol preparation method

-

Paragraph 0021; 0024; 0029; 0034, (2018/06/14)

The invention relates to the field of organic synthesis, discloses a 1, 2, 3, 4 - four-toluol preparation method, comprising: step 1:1, 7 - dimethyl - 4, 10 - dioxa - tricyclic [5.2.1 . 0] becc - 8 - 8 en - 3, 5 - dione synthetic; step 2:4, 7 - dimethyl - isobenzofuran - 1, 3 - dione synthetic; step 3:1, 2 - double-(hydroxy methyl) - 3, 6 - dimethylphenyl synthetic; step 4:1, 2 - (bromomethyl)-- 3, 6 - dimethylphenyl synthetic; step 5: 1, 2, 3, 4 - four-toluol synthesis. The invention to maleic anhydride, 2, 5 - dimethyl furan as raw materials, high purity of the 1, 2, 3, 4 - tetramethyl-benzene, this method has no high-temperature high-pressure and other dangerous reaction conditions, is not of a special material, and will not synthetic 1, 2, 4, 5 - substances such as tetramethyl-benzene, the final product does not need to follow-up separation, is suitable for industrial production.

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

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

supporting information; experimental part, 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

High performance, acene-based organic thin film transistors

Llorente, Gonzalo Rincon,Dufourg-Madec, Marie-Beatrice,Crouch, David J.,Pritchard, Robin G.,Ogier, Simon,Yeates, Stephen G.

supporting information; experimental part, p. 3059 - 3061 (2009/12/01)

1,4,8,11-Methyl-substituted 6,13-triethylsilylethynylpentacene shows extended π-π overlap when deposited from solution, yielding organic thin film transistors with high and reproducible hole mobility with negligible hysteresis. The Royal Society of Chemis

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.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 38108-82-6