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Benzene, 1,2,4,5-tetrabromo-3-(bromomethyl)-6-methyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

66217-03-6

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66217-03-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 66217-03-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,6,2,1 and 7 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 66217-03:
(7*6)+(6*6)+(5*2)+(4*1)+(3*7)+(2*0)+(1*3)=116
116 % 10 = 6
So 66217-03-6 is a valid CAS Registry Number.

66217-03-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,2,4,5-tetrabromo-3-(bromomethyl)-6-methylbenzene

1.2 Other means of identification

Product number -
Other names Benzene,1,2,4,5-tetrabromo-3-(bromomethyl)-6-methyl

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:66217-03-6 SDS

66217-03-6Upstream product

66217-03-6Downstream Products

66217-03-6Relevant academic research and scientific papers

An improved method for the regiospecific synthesis of polysubstituted [2.2]paracyclophanes

Chow, Hak-Fun,Low, Kam-Hung,Wong, King Y.

, p. 2130 - 2134 (2005)

4,16-Disubstituted, 4,7,12,15-tetrasubstituted, 4,8,12,16-tetrasubstituted and 4,5,7,8,12,13,15,16-octasubstituted [2.2]paracyclophanes can be prepared in significantly improved yields and excellent regiospecificities via the Winberg 1,6-elimination-dimerization reaction from substituted (4-methylbenzyl) trimethylammonium hydroxides. Using 2-chloro-phenothiazine instead of phenothiazine as a polymerization inhibitor results in a doubling of product yields. Georg Thieme Verlag Stuttgart.

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