79247-92-0 Usage
Uses
Used in Pharmaceutical Industry:
4-Phenyl-thiazole-2-carboxylic acid ethyl ester serves as a crucial building block in the synthesis of a wide array of drugs and pharmaceutical products. Its role in organic synthesis and medicinal chemistry is significant, as it can be employed as a starting material for the preparation of compounds that exhibit potential biological activity. This makes it a valuable component in the development of new therapeutic agents.
Used in Organic Synthesis:
In the realm of organic synthesis, 4-Phenyl-thiazole-2-carboxylic acid ethyl ester is utilized as a key intermediate for creating various complex organic molecules. Its reactivity and structural features facilitate the formation of diverse chemical entities, contributing to the advancement of organic chemistry.
Used in Flavor and Fragrance Industry:
Beyond its applications in pharmaceuticals and organic synthesis, 4-Phenyl-thiazole-2-carboxylic acid ethyl ester also finds use in the food industry as a flavor and fragrance ingredient. Its unique aromatic properties allow it to enhance the sensory experience of food products, adding depth and complexity to their taste and smell profiles.
Check Digit Verification of cas no
The CAS Registry Mumber 79247-92-0 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, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 79247-92:
(7*7)+(6*9)+(5*2)+(4*4)+(3*7)+(2*9)+(1*2)=170
170 % 10 = 0
So 79247-92-0 is a valid CAS Registry Number.
79247-92-0Relevant academic research and scientific papers
RING-SELECTIVE PHOTOREARRANGEMENT OF BITHIAZOLES
Saito, Isao,Morii, Takashi,Okumura, Yukihisa,Mori, Satoru,Yamaguchi, Kizashi,Matsuura, Teruo
, p. 6385 - 6388 (2007/10/02)
Photoirradiation of methyl 2'-methyl-2,4'-bithiazole-4-carboxylate (1) leads predominantly to 4,4'-bithiazole 2 with the formation of a small amount of isothiazole 3.The ring-selective photorearrangement is interpreted in terms of LUMO bond index.
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.
