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(4-Bromothiazol-2-yl)methanamine, also known as 2-amino-4-bromothiazole, is a chemical compound with the molecular formula C4H5BrN2S. It is a brominated derivative of thiazole, characterized by its unique structure and properties. (4-BroMothiazol-2-yl)MethanaMine is widely used in the pharmaceutical and chemical industries for the synthesis of various compounds, including antimicrobial and antifungal agents, as well as heterocyclic compounds. Its versatility and potential applications make it a valuable component in the development of novel drugs and other chemical products.

697299-86-8

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697299-86-8 Usage

Uses

Used in Pharmaceutical Industry:
(4-Bromothiazol-2-yl)methanamine is used as a key intermediate in the synthesis of various pharmaceutical compounds. Its unique structure and properties make it a promising candidate for the development of novel drugs with potential therapeutic applications.
Used in Antimicrobial and Antifungal Applications:
(4-Bromothiazol-2-yl)methanamine exhibits antimicrobial and antifungal properties, making it a valuable component in the development of new antimicrobial and antifungal agents. These agents can be used to combat various infections caused by bacteria and fungi, offering potential solutions to the growing problem of antibiotic resistance.
Used in Chemical Industry:
In the chemical industry, (4-Bromothiazol-2-yl)methanamine serves as a building block in the synthesis of heterocyclic compounds. These compounds are important in various applications, including the development of agrochemicals, dyes, and other specialty chemicals.
Used in Agrochemical Production:
(4-Bromothiazol-2-yl)methanamine can be utilized in the production of agrochemicals, such as pesticides and herbicides. Its incorporation into these products can enhance their effectiveness in controlling pests and diseases in agricultural settings, contributing to increased crop yields and food security.
Used in Dye Production:
(4-BroMothiazol-2-yl)MethanaMine can also be used in the synthesis of dyes, which are essential in various industries, including textiles, plastics, and printing. Its unique properties can contribute to the development of new dyes with improved colorfastness, brightness, and other desirable characteristics.

Check Digit Verification of cas no

The CAS Registry Mumber 697299-86-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,9,7,2,9 and 9 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 697299-86:
(8*6)+(7*9)+(6*7)+(5*2)+(4*9)+(3*9)+(2*8)+(1*6)=248
248 % 10 = 8
So 697299-86-8 is a valid CAS Registry Number.

697299-86-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name (4-bromo-1,3-thiazol-2-yl)methanamine

1.2 Other means of identification

Product number -
Other names (4-Bromo-thiazol-2-yl)-methylamine

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:697299-86-8 SDS

697299-86-8Relevant academic research and scientific papers

IMIDOTHIAZOLE KINASE INHIBITORS

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Page/Page column 55-57, (2011/04/24)

The present invention is directed to novel kinase inhibitors of general formula (I) and pharmaceutically acceptable salts thereof, and to the use of the kinase inhibitors of general formula (I) for treating diseases or disorders in which tau phosphorylati

Cyanoguanidines and cyanoamidines as ErbB2 and EGFR inhibitors

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Page/Page column 10, (2008/06/13)

Cyanoguanidine quinazoline and cyanoamidine quinazolamine derivatives that are useful in the treatment of hyperproliferative diseases are disclosed. Methods of treating hyperproliferative diseases in mammals are also disclosed.

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