79247-98-6 Usage
Uses
Used in Flavoring Agents:
Methyl 5-methyl-1,3-thiazole-2-carboxylate is used as a flavoring agent in the food and beverage industry for its distinctive fruity and earthy aroma, enhancing the taste and smell of various products.
Used in Pharmaceutical Synthesis:
In the pharmaceutical industry, methyl 5-methyl-1,3-thiazole-2-carboxylate is utilized as a key intermediate in the synthesis of various drugs, leveraging its unique chemical properties to contribute to the development of new medicinal compounds.
Used in Agrochemical Synthesis:
Similarly, in the agrochemical sector, methyl 5-methyl-1,3-thiazole-2-carboxylate serves as an important building block in the creation of different agrochemicals, playing a role in the development of products designed to protect and enhance crop yields and quality.
Used in Fragrance Industry:
Methyl 5-methyl-1,3-thiazole-2-carboxylate is also employed in the fragrance industry to create unique scents for a variety of products, from perfumes to household items, capitalizing on its naturally occurring fruity and earthy notes.
Check Digit Verification of cas no
The CAS Registry Mumber 79247-98-6 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 8 respectively.
Calculate Digit Verification of CAS Registry Number 79247-98:
(7*7)+(6*9)+(5*2)+(4*4)+(3*7)+(2*9)+(1*8)=176
176 % 10 = 6
So 79247-98-6 is a valid CAS Registry Number.
79247-98-6Relevant 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.
