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2-Benzothiazolamine,4-chloro-6-fluoro-(9CI) is a chemical compound with the molecular formula C7H4ClFN2S. It is a derivative of benzothiazole and contains a chlorine and a fluorine atom. 2-Benzothiazolamine,4-chloro-6-fluoro-(9CI) has potential applications in various fields due to its versatile properties.

210834-98-3

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210834-98-3 Usage

Uses

Used in Pharmaceutical Industry:
2-Benzothiazolamine,4-chloro-6-fluoro-(9CI) is used as a building block for the synthesis of new compounds with valuable biological activities. It serves as an important intermediate in the development of novel chemical entities for pharmaceutical applications.
Used in Agrochemical Industry:
In the agrochemical industry, 2-Benzothiazolamine,4-chloro-6-fluoro-(9CI) is utilized as a key component in the creation of new compounds with potential pesticidal or herbicidal properties, contributing to the development of more effective and environmentally friendly agrochemicals.
Used in Material Science:
2-Benzothiazolamine,4-chloro-6-fluoro-(9CI) also finds application in material science, where it is used to synthesize new materials with unique properties. These materials can be employed in various technological applications, such as in the development of advanced coatings, sensors, or other innovative products.

Check Digit Verification of cas no

The CAS Registry Mumber 210834-98-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,0,8,3 and 4 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 210834-98:
(8*2)+(7*1)+(6*0)+(5*8)+(4*3)+(3*4)+(2*9)+(1*8)=113
113 % 10 = 3
So 210834-98-3 is a valid CAS Registry Number.
InChI:InChI=1/C7H4ClFN2S/c8-4-1-3(9)2-5-6(4)11-7(10)12-5/h1-2H,(H2,10,11)

210834-98-3 Well-known Company Product Price

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  • Aldrich

  • (CBR01457)  4-Chloro-6-fluoro-1,3-benzothiazol-2-amine  AldrichCPR

  • 210834-98-3

  • CBR01457-1G

  • 2,575.17CNY

  • Detail

210834-98-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-chloro-6-fluoro-1,3-benzothiazol-2-amine

1.2 Other means of identification

Product number -
Other names 2-Amino-4-chloro-6-fluorobenzothiazole

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:210834-98-3 SDS

210834-98-3Relevant academic research and scientific papers

Antiproliferative activity evaluation of a series of N-1,3-benzothiazol-2-ylbenzamides as novel apoptosis inducers

Corbo, Filomena,Carocci, Alessia,Armenise, Domenico,De Laurentis, Nicolino,Laghezza, Antonio,Loiodice, Fulvio,Ancona, Patrizia,Muraglia, Marilena,Pagliarulo, Vincenzo,Franchini, Carlo,Catalano, Alessia

, (2016)

A series of N-1,3-benzothiazol-2-ylbenzamide derivatives were studied for their antiproliferative activity on human liver hepatocellular carcinoma (HepG2) and human breast cancer (MCF-7) cell lines. Most of them were found to show a prominent inhibitory e

BICYCLIC HETEROARYL SUBSTITUTED COMPOUNDS

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Page/Page column 688; 690, (2018/03/25)

Disclosed are compounds of Formula (I) to (VIII): (I) (II) (III) (IV) (V) (VI) (VII) (VIII); or a stereoisomer, tautomer, pharmaceutically acceptable salt, solvate or prodrug thereof, wherein R3 is a bicyclic heteroaryl group substituted with zero to 3 R3a; and R1, R2, R3a, R4, and n are defined herein. Also disclosed are methods of using such compounds as PAR4 inhibitors, and pharmaceutical compositions comprising such compounds. These compounds are useful in inhibiting or preventing platelet aggregation, and are useful for the treatment of a thromboembolic disorder or the primary prophylaxis of a thromboembolic disorder.

Synthesis and antifungal activity against strains of Candida albicans of 6-fluoro-4(5 or 7)-chloro-2-(difluorobenzoyl)aminobenzothiazoles

Armenise, Domenico,De Laurentis, Nicolino,Reho, Antonia,Rosato, Antonio,Morlacchi, Flaviano

, p. 771 - 775 (2007/10/03)

A series of 6-fluoro-4-(5 or 7)-chloro-2-(difluorobenzoyl) aminobenzothiazoles 3a-r were prepared to investigate their potential biological activity. In this work, the results of their in vitro antifungal activity against some strains of Candida albicans

Substituted benzothiazols with herbicidal action

-

, (2008/06/13)

Substituted benzothiazoles I and their salts STR1 used as herbicides and for the desiccation/abscission of plants.

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