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2-Thiazolecarboxylic acid, 5-ethylis a chemical compound with the molecular formula C7H7NO2S and a molecular weight of 173.2 g/mol. It is a derivative of thiazolecarboxylic acid with an ethyl group attached to the fifth position of the thiazole ring. 2-Thiazolecarboxylic acid, 5-ethylis known for its potential antioxidant and antimicrobial properties, as well as its role as a building block in the synthesis of pharmaceuticals and agrochemicals. It is also investigated for its use in the development of new materials and as a precursor in organic synthesis, making it significant in the fields of medicinal chemistry and material science.

75954-20-0

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75954-20-0 Usage

Uses

Used in Pharmaceutical Industry:
2-Thiazolecarboxylic acid, 5-ethylis used as a building block for the synthesis of various pharmaceuticals due to its unique chemical structure and properties. Its presence in the development of new drugs can contribute to the discovery of novel therapeutic agents.
Used in Agrochemical Industry:
In the agrochemical industry, 2-Thiazolecarboxylic acid, 5-ethylserves as a key component in the synthesis of agrochemicals, potentially leading to the creation of new pesticides or other agricultural products that can improve crop protection and yield.
Used in Material Science:
2-Thiazolecarboxylic acid, 5-ethylis utilized in the development of new materials, where its chemical properties can enhance the performance or introduce new functionalities to existing materials.
Used as an Antioxidant:
2-Thiazolecarboxylic acid, 5-ethylis studied for its potential antioxidant properties, which can be beneficial in various applications, such as in the food industry to extend the shelf life of products or in cosmetic products to protect against oxidative stress.
Used as an Antimicrobial Agent:
2-Thiazolecarboxylic acid, 5-ethylis also investigated for its antimicrobial properties, which can be applied in different industries, such as healthcare for the development of new antibiotics or in the food industry to prevent spoilage and contamination.
Used in Organic Synthesis:
As a precursor in organic synthesis, 2-Thiazolecarboxylic acid, 5-ethylplays a crucial role in the creation of a wide range of organic compounds, contributing to the advancement of chemical research and the development of new chemical products.

Check Digit Verification of cas no

The CAS Registry Mumber 75954-20-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,9,5 and 4 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 75954-20:
(7*7)+(6*5)+(5*9)+(4*5)+(3*4)+(2*2)+(1*0)=160
160 % 10 = 0
So 75954-20-0 is a valid CAS Registry Number.

75954-20-0SDS

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-ethyl-1,3-thiazole-2-carboxylic acid

1.2 Other means of identification

Product number -
Other names 2-thiazolecarboxylic acid,5-ethyl

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:75954-20-0 SDS

75954-20-0Downstream Products

75954-20-0Relevant 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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