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1188227-29-3

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1188227-29-3 Usage

Description

7-Bromo-2-chlorobenzothiazole is a heterocyclic chemical compound belonging to the benzothiazole family. It features a benzene ring fused to a thiazole ring, with a bromine and a chlorine substituent attached. 7-BroMo-2-chlorobenzothiazole is known for its versatile chemical properties and applications in various industries.

Uses

Used in Pharmaceutical Industry:
7-Bromo-2-chlorobenzothiazole is used as a building block for the synthesis of pharmaceuticals. Its unique structure and functional groups make it a valuable component in the development of new drugs with potential therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical industry, 7-Bromo-2-chlorobenzothiazole serves as a key intermediate in the production of agrochemicals. Its chemical properties allow it to be incorporated into compounds that can be used for pest control, crop protection, and other agricultural purposes.
Used in Dye Industry:
7-Bromo-2-chlorobenzothiazole is utilized as a building block in the synthesis of dyes. Its ability to form stable chemical bonds with other molecules contributes to the creation of dyes with specific color properties and stability.
Used in Organic Synthesis:
7-Bromo-2-chlorobenzothiazole is used as a reagent in organic synthesis reactions. Its presence in various chemical processes allows for the formation of new compounds with desired properties, making it a valuable tool in the synthesis of organic compounds.
Used in Industrial Applications:
As a key intermediate, 7-Bromo-2-chlorobenzothiazole is used in the manufacturing of materials for industrial applications. Its chemical properties enable it to be incorporated into materials with specific characteristics, such as improved stability, durability, or functionality.
Used in Research Laboratories:
7-Bromo-2-chlorobenzothiazole is employed as a research chemical in laboratories. Its unique structure and properties make it an interesting subject for scientific investigations, contributing to the advancement of knowledge in the field of chemistry and related disciplines.

Check Digit Verification of cas no

The CAS Registry Mumber 1188227-29-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,8,8,2,2 and 7 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1188227-29:
(9*1)+(8*1)+(7*8)+(6*8)+(5*2)+(4*2)+(3*7)+(2*2)+(1*9)=173
173 % 10 = 3
So 1188227-29-3 is a valid CAS Registry Number.

1188227-29-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 7-Bromo-2-chloro-1,3-benzothiazole

1.2 Other means of identification

Product number -
Other names 2-CHLORO-7-BROMOBENZOTHIAZOLE

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:1188227-29-3 SDS

1188227-29-3Downstream Products

1188227-29-3Relevant articles and documents

Small-compound enhancers for functional O-mannosylation of alpha-dystroglycan, and uses thereof

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Page/Page column 24; 25, (2019/03/14)

The present invention provides compounds that can enhance functional O-mannosylation of proteins including alpha-dystroglycan. Also provided are methods of preparation of the compounds defined by the formula I. Also provided are the methods of using the compounds or the pharmaceutical acceptable salts or prodrugs thereof in treating and preventing subjects suffering from the diseases including muscular dystrophies and cancers.

7-AMINOFUROPYRIDINE DERIVATIVES

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Page/Page column 56, (2011/09/15)

Compounds of Formula 1, as shown below and defined herein: pharmaceutically acceptable salts thereof, synthesis, intermediates, formulations, and methods of disease treatment therewith, including treatment of cancers, such as tumors driven at least in part by TAK1 or for which an appropriate TAK1 inhibitor is effective. This Abstract is not limiting of the invention.

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