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5-(4-Bromophenyl)Isothiazole is a chemical compound that belongs to the class of organic compounds known as aryl halides. It is an isothiazole compound with a bromophenyl group attached to it. Isothiazoles are sulfur, nitrogen containing heterocycles similar to thiazoles but with a different atom arrangement. The prefix "4-Bromo" indicates the position of the bromine atom on the phenyl ring. Due to its reactive nature, it could serve a role in various chemical reactions, although its specific applications and toxicity are not widely mentioned in the available literature, suggesting that it might be primarily used in research contexts.

49602-97-3

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49602-97-3 Usage

Uses

Used in Chemical Reactions:
5-(4-Bromophenyl)Isothiazole is used as a reactive compound for various chemical reactions due to its aryl halide nature. Its potential applications in synthesis and modification of other compounds make it a valuable compound in the field of organic chemistry.
Used in Research Contexts:
5-(4-Bromophenyl)Isothiazole is used as a research compound for studying its properties, reactivity, and potential applications in different chemical processes. As its specific uses and toxicity are not well-documented, it is primarily utilized in controlled research environments to explore its potential benefits and safety concerns.
Used in Pharmaceutical Research:
5-(4-Bromophenyl)Isothiazole is used as a starting material or intermediate in the synthesis of pharmaceutical compounds. Its unique structure and reactivity may contribute to the development of new drugs or drug candidates, although further research is needed to establish its safety and efficacy in this context.
Used in Material Science:
5-(4-Bromophenyl)Isothiazole is used as a component in the development of new materials with specific properties, such as electronic, optical, or mechanical characteristics. Its incorporation into various materials may lead to the creation of novel materials with improved performance in different applications.
Note: Due to the limited information available on the toxicity and safety of 5-(4-Bromophenyl)Isothiazole, it is essential to take appropriate safety measures while handling 5-(4-BROMOPHENYL) ISOTHIAZOLE until thorough studies on its toxicity and safety are carried out.

Check Digit Verification of cas no

The CAS Registry Mumber 49602-97-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,9,6,0 and 2 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 49602-97:
(7*4)+(6*9)+(5*6)+(4*0)+(3*2)+(2*9)+(1*7)=143
143 % 10 = 3
So 49602-97-3 is a valid CAS Registry Number.

49602-97-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-(4-BROMOPHENYL) ISOTHIAZOLE

1.2 Other means of identification

Product number -
Other names 5-(4-Bromophenyl)isothiazole

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:49602-97-3 SDS

49602-97-3Relevant academic research and scientific papers

New Synthesis of Isoxazoles and Isothiazoles. A Convenient Synthesis of Thioenaminones from Enaminones

Lin, Yang-i,Lang, Stanley, A.

, p. 4857 - 4860 (2007/10/02)

The reaction of 1-aryl-3-(dimethylamino)-2-propene-1-ones (enaminones) and 1-aryl-3-(dimethylamino)-2-propene-1-thiones (thioenaminones) with hydroxylamine-O-sulfonic acid gave, respectively, isoxazoles in 76-84 percent yields and isothiazoles in 60-65 pe

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