79247-85-1 Usage
Uses
Used in Pharmaceutical Industry:
2-Thiazolecarboxylic acid, 4-(trifluoromethyl)-, methyl ester is used as a building block in the synthesis of various drugs and pharmaceutical compounds. Its unique structure, including the thiazole ring and trifluoromethyl group, contributes to the development of new therapeutic agents with improved pharmacological properties.
Used in Pesticide or Fungicide Development:
Due to its thiazole ring, which is known for its bioactivity, 2-Thiazolecarboxylic acid, 4-(trifluoromethyl)-, methyl ester has potential use as a pesticide or fungicide. Its ability to interact with biological targets can be leveraged to create effective agents for controlling pests and fungi in agriculture.
Used in Organic Synthesis:
2-Thiazolecarboxylic acid, 4-(trifluoromethyl)-, methyl ester can be used as a starting material in organic synthesis for the preparation of various other chemical compounds. Its versatile structure allows for further functionalization and modification, enabling the creation of a wide range of molecules with diverse applications in various fields.
Check Digit Verification of cas no
The CAS Registry Mumber 79247-85-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,2,4 and 7 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 79247-85:
(7*7)+(6*9)+(5*2)+(4*4)+(3*7)+(2*8)+(1*5)=171
171 % 10 = 1
So 79247-85-1 is a valid CAS Registry Number.
79247-85-1Relevant 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.
