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4-(4-BROMO-PHENYL)-THIAZOLE-2-CARBOXYLIC ACID is a chemical compound characterized by the molecular formula C11H7BrNO2S. It is a thiazole derivative featuring a carboxylic acid group and a bromo-substituted phenyl ring. 4-(4-BROMO-PHENYL)-THIAZOLE-2-CARBOXYLIC ACID is recognized for its potential biological activities, including antimicrobial, antifungal, and antitumor properties. Its versatile chemical structure and functional groups render it a valuable starting material for the development of new pharmaceuticals and other bioactive compounds.

886366-94-5

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886366-94-5 Usage

Uses

Used in Pharmaceutical Industry:
4-(4-BROMO-PHENYL)-THIAZOLE-2-CARBOXYLIC ACID is used as a building block or precursor in organic synthesis for the production of pharmaceuticals. Its unique structure and functional groups contribute to the development of new and improved drugs with enhanced therapeutic effects.
Used in Agrochemical Industry:
In the agrochemical sector, 4-(4-BROMO-PHENYL)-THIAZOLE-2-CARBOXYLIC ACID is utilized as a starting material for the synthesis of agrochemicals. Its antimicrobial and antifungal properties make it a promising candidate for the development of effective pesticides and fungicides.
Used in Fine Chemicals Industry:
4-(4-BROMO-PHENYL)-THIAZOLE-2-CARBOXYLIC ACID is also employed in the synthesis of other fine chemicals. Its versatility and potential biological activities allow for the creation of a wide range of specialty chemicals for various applications.
Used in Antimicrobial Applications:
4-(4-BROMO-PHENYL)-THIAZOLE-2-CARBOXYLIC ACID is used as an antimicrobial agent for its ability to inhibit the growth of various microorganisms. This property makes it suitable for use in the development of new antimicrobial drugs and treatments.
Used in Antifungal Applications:
4-(4-BROMO-PHENYL)-THIAZOLE-2-CARBOXYLIC ACID is utilized as an antifungal agent, leveraging its ability to combat fungal infections. Its incorporation into antifungal medications can help address various fungal-related health issues.
Used in Antitumor Applications:
4-(4-BROMO-PHENYL)-THIAZOLE-2-CARBOXYLIC ACID is employed in antitumor research and drug development due to its demonstrated antitumor properties. Its potential to inhibit tumor growth and progression makes it a valuable component in the creation of novel cancer therapies.

Check Digit Verification of cas no

The CAS Registry Mumber 886366-94-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,6,3,6 and 6 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 886366-94:
(8*8)+(7*8)+(6*6)+(5*3)+(4*6)+(3*6)+(2*9)+(1*4)=235
235 % 10 = 5
So 886366-94-5 is a valid CAS Registry Number.

886366-94-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(4-bromophenyl)-1,3-thiazole-2-carboxylic acid

1.2 Other means of identification

Product number -
Other names 4-(4-Bromophenyl)thiazole-2-carboxylicAcid

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:886366-94-5 SDS

886366-94-5Relevant academic research and scientific papers

An Infrared Study of Rotational Isomerism in Thiazole-2-carboxylates

Kaye, Perry T.,Meakins, G. Denis,Willbe, Charles,Williams, Peter R.

, p. 2335 - 2339 (2007/10/02)

A series of alkyl thiazole-2-carboxylates containing a range of substituents at the 4- and 5-positions has been prepared.Solutions of these esters (mostly new compounds) show well resolved doublets in the i.r.C=O region which arise from rotational isomers.The higher wavenumber components are assigned to the more polar carbonyl O,S-anti-s-trans-rotamers and the lower wavenumber components to the carbonyl O,S-syn-s-trans-forms.Small, but systematic, differences between the methyl esters are noted.

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