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2-Bromo-5-chlorobenzothiazole is a chemical compound that features a benzothiazole core with bromine and chlorine atoms attached at the 2nd and 5th positions, respectively. 2-Bromo-5-chlorobenzothiazole is recognized for its potential applications across various industries due to its unique structural and functional properties.

2941-56-2

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2941-56-2 Usage

Uses

Used in Pharmaceutical Industry:
2-Bromo-5-chlorobenzothiazole is used as a building block for the synthesis of pharmaceuticals, leveraging its chemical structure to create new drugs with specific therapeutic properties. Its antimicrobial and antifungal properties make it a promising candidate for the development of novel antimicrobial agents to combat resistant strains of bacteria and fungi.
Used in Agrochemical Industry:
In the agrochemical sector, 2-Bromo-5-chlorobenzothiazole is utilized as a precursor in the synthesis of pesticides. Its antimicrobial and antifungal characteristics contribute to the development of effective crop protection products, enhancing agricultural yields and food security.
Used in Specialty Chemicals:
2-Bromo-5-chlorobenzothiazole serves as a key component in the production of specialty chemicals, where its unique chemical properties are harnessed to create compounds with specific applications in various industries, such as dyes, plastics, and coatings.
Used in Corrosion Inhibition:
2-Bromo-5-chlorobenzothiazole is investigated for its potential as a corrosion inhibitor for metal surfaces. Its ability to form protective layers on metal surfaces can help prevent corrosion, extending the lifespan of metal structures and components in various applications, including automotive, aerospace, and construction industries.
It is crucial to handle 2-Bromo-5-chlorobenzothiazole with care due to its hazardous nature, which may cause skin, eye, and respiratory irritation. Proper safety measures should be implemented during its production, use, and disposal to minimize potential health and environmental risks.

Check Digit Verification of cas no

The CAS Registry Mumber 2941-56-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,9,4 and 1 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 2941-56:
(6*2)+(5*9)+(4*4)+(3*1)+(2*5)+(1*6)=92
92 % 10 = 2
So 2941-56-2 is a valid CAS Registry Number.
InChI:InChI=1/C7H3BrClNS/c8-7-10-5-3-4(9)1-2-6(5)11-7/h1-3H

2941-56-2SDS

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-Bromo-5-chloro-1,3-benzothiazole

1.2 Other means of identification

Product number -
Other names 2-Brom-5-chlor-benzothiazol

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:2941-56-2 SDS

2941-56-2Downstream Products

2941-56-2Relevant academic research and scientific papers

Design, synthesis, and SAR of cis-1,2-diaminocyclohexane derivatives as potent factor Xa inhibitors. Part I: Exploration of 5-6 fused rings as alternative S1 moieties

Yoshikawa, Kenji,Yokomizo, Aki,Naito, Hiroyuki,Haginoya, Noriyasu,Kobayashi, Shozo,Yoshino, Toshiharu,Nagata, Tsutomu,Mochizuki, Akiyoshi,Osanai, Ken,Watanabe, Kengo,Kanno, Hideyuki,Ohta, Toshiharu

experimental part, p. 8206 - 8220 (2010/04/06)

A series of cis-1,2-diaminocyclohexane derivatives were synthesized with the aim of optimizing previously disclosed factor Xa (fXa) inhibitors. The exploration of 5-6 fused rings as alternative S1 moieties resulted in two compounds which demonstrated improved solubility and reduced food effect compared to the clinical candidate, compound A. Herein, we describe the synthesis and structure-activity relationship (SAR), together with the physicochemical properties and pharmacokinetic (PK) profiles of some prospective compounds.

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