58334-08-0 Usage
General Description
Ethyl 5-methylthiazole-2-carboxylate is a chemical compound with a molecular formula C8H11NO2S. It is commonly used in the synthesis of pharmaceuticals and agrochemicals due to its unique chemical structure and potential biological activities. Ethyl 5-methylthiazole-2-carboxylate has a thiazole ring with an ethyl ester side chain, and its presence imparts a distinct odor to the substances it is used in. Ethyl 5-methylthiazole-2-carboxylate is also utilized as a flavoring agent in the food industry, adding a savory and meaty taste to various products. Overall, this compound has diverse applications in the fields of chemistry, medicine, and food science.
Check Digit Verification of cas no
The CAS Registry Mumber 58334-08-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,3,3 and 4 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 58334-08:
(7*5)+(6*8)+(5*3)+(4*3)+(3*4)+(2*0)+(1*8)=130
130 % 10 = 0
So 58334-08-0 is a valid CAS Registry Number.
58334-08-0Relevant articles and documents
MRGPRX2 ANTAGONISTS FOR THE TREATMENT OF INFLAMMATORY DISORDERS
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Paragraph 00115; 00212-00214, (2021/05/15)
The present disclosure is directed to use of MrgprX2 antagonists in the treatment of inflammatory disorders, e.g., inflammatory disorders of the skin. This invention is also directed to pharmaceutical compositions comprising a MrgprX2 antagonist and a pha
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.
