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112146-10-8

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112146-10-8 Usage

General Description

4-Bromo-2-methylbenzothiazole, also known as BM-MBT, is a chemical compound with the molecular formula C8H6BrNS. It is a white to light yellow solid that is used as a building block in the synthesis of various pharmaceuticals, agrochemicals, and dyes. 4-Bromo-2-methylbenzothiazole is also utilized as an intermediate in the production of rubber chemicals and additives. 4-BROMO-2-METHYLBENZOTHIAZOLE is known to be a skin and eye irritant, and should be handled with caution. Additionally, it is considered to be potentially harmful to aquatic organisms, and proper disposal methods should be employed to prevent environmental contamination.

Check Digit Verification of cas no

The CAS Registry Mumber 112146-10-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,2,1,4 and 6 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 112146-10:
(8*1)+(7*1)+(6*2)+(5*1)+(4*4)+(3*6)+(2*1)+(1*0)=68
68 % 10 = 8
So 112146-10-8 is a valid CAS Registry Number.

112146-10-8SDS

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 4-Bromo-2-methylbenzo[d]thiazole

1.2 Other means of identification

Product number -
Other names 4-bromo-2-methyl-1,3-benzothiazole

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:112146-10-8 SDS

112146-10-8Upstream product

112146-10-8Downstream Products

112146-10-8Relevant articles and documents

Regioselective one-pot synthesis of 2-aryl-6-bromobenzothiazole from arylaldehyde and 2-aminothiophenol with phenyltrimethylammonium tribromide in the presence of a catalytic amount of antimony(III) bromide

Sayama, Shinsei

experimental part, p. 1267 - 1274 (2011/06/27)

Various 2-aryl-6-bromo-1,3-benzothiazoles were regioselectively afforded in good yields by the reaction of arylaldehydes and 2-aminothiophenol with phenyltrimethylammonium tribromide in the presence of a catalytic amount of SbBr3 in CH2Cl2 at room temperature.

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