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2-ethyl-1,3-thiazole-5-carboxylic acid is a chemical compound characterized by its molecular formula C7H9NO2S. It is a derivative of thiazole, featuring an ethyl group and a carboxylic acid group within its structure. 2-ethyl-1,3-thiazole-5-carboxylic acid is known for its strong odor and is recognized for its versatility in chemical reactions, making it a valuable component in the synthesis of various products, including flavorings, pharmaceuticals, and agrochemicals. Its potential extends to the development of new materials and research in organic chemistry.

30709-68-3

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30709-68-3 Usage

Uses

Used in Flavoring Industry:
2-ethyl-1,3-thiazole-5-carboxylic acid is used as a flavoring agent due to its strong odor, contributing to the creation of distinct tastes and scents in food and beverage products.
Used in Pharmaceutical Industry:
In the pharmaceutical sector, 2-ethyl-1,3-thiazole-5-carboxylic acid serves as a key intermediate in the synthesis of various drugs, leveraging its chemical properties to form new medicinal compounds.
Used in Agrochemical Industry:
2-ethyl-1,3-thiazole-5-carboxylic acid is utilized in the development of agrochemicals, where its chemical structure aids in the creation of effective pesticides and other agricultural products.
Used in Material Science:
2-ethyl-1,3-thiazole-5-carboxylic acid is employed in the field of material science for the development of new materials, taking advantage of its reactive groups to form novel substances with unique properties.
Used in Organic Chemistry Research:
2-ethyl-1,3-thiazole-5-carboxylic acid is used as a research compound in organic chemistry, where its participation in various chemical reactions helps in understanding and advancing the field of chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 30709-68-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,0,7,0 and 9 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 30709-68:
(7*3)+(6*0)+(5*7)+(4*0)+(3*9)+(2*6)+(1*8)=103
103 % 10 = 3
So 30709-68-3 is a valid CAS Registry Number.
InChI:InChI=1/C6H7NO2S/c1-2-5-7-3-4(10-5)6(8)9/h3H,2H2,1H3,(H,8,9)

30709-68-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Ethyl-1,3-thiazole-5-carboxylic acid

1.2 Other means of identification

Product number -
Other names 2-ethyl-5-carboxythiazole

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:30709-68-3 SDS

30709-68-3Relevant academic research and scientific papers

SUBSTITUTED AMINOPROPIONIC DERIVATIVES AS NEPRILYSIN INHIBITORS

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Page/Page column 237, (2010/12/26)

The present invention provides a compound of formula I' or a pharmaceutically acceptable salt thereof, wherein R1, R2, R3, R5, B1, X and n are defined herein. The invention also relates a method for manufacturing the compounds of the invention, and its therapeutic uses. The present invention further provides a combination of pharmacologically active agents and a pharmaceutical composition.

2-Alkyl-5-thiazole-carboxylic acid derivatives in hypolipemiant compositions

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, (2008/06/13)

Hypolipemiant compositions comprising an effective amount of at least one 2-alkyl-5-thiazole-carboxylic acid derivative of the formula STR1 wherein R is hydrogen, an alkali metal, ammonium, the monovalent residue of an organic base or a substituted or unsubstituted alkyl and where R'1 is a linear alkyl of 1 to 12 carbon atoms, and a major amount of a pharmaceutical carrier; as well as the method of reducing the amount of sanguine lipids in warm-blooded animals utilizing the above-hypolipemiant compositions.

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