13950-67-9 Usage
Uses
Used in Pharmaceutical Industry:
2,3-Dihydro-2-oxo-4-phenyl-5-thiazolecarboxylic acid ethyl ester is used as a key intermediate in the synthesis of various drugs. Its unique chemical structure allows it to be a versatile building block for the development of new pharmaceutical compounds.
Used in Drug Development:
2,3-Dihydro-2-oxo-4-phenyl-5-thiazolecarboxylic acid ethyl ester has potential therapeutic applications due to its ability to inhibit certain enzymes or interact with specific biological targets. This makes it a promising candidate in the development of medications for a variety of medical conditions, including but not limited to, inflammatory diseases, neurological disorders, and cancer.
Used in Chemical Production:
In addition to its pharmaceutical applications, 2,3-Dihydro-2-oxo-4-phenyl-5-thiazolecarboxylic acid ethyl ester may also have industrial uses in the production of various chemicals and materials. Its unique chemical properties can contribute to the development of new chemical products and materials with specific applications in different industries.
Check Digit Verification of cas no
The CAS Registry Mumber 13950-67-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,9,5 and 0 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 13950-67:
(7*1)+(6*3)+(5*9)+(4*5)+(3*0)+(2*6)+(1*7)=109
109 % 10 = 9
So 13950-67-9 is a valid CAS Registry Number.
13950-67-9Relevant academic research and scientific papers
Synthesis and characteristics of novel thiazoie and dithiazole derivatives. Reactions of acyclic- and heterocyclic Cis-disulfides with some nucleophilic phosphorus reagents
Abdou, Wafaa M.
, p. 393 - 396 (2007/10/03)
The behavior of phosphorus ylides such as alkoxycarbonyl- and β-ketoalkylidenephosphoranes toward different types of acyclic and cyclic cis-disulfides has been investigated whereby several substituted-thiazoles, dithiazoles, thioles and dithioles as well
Syntheses and Reactions of 2-Halo-5-thiazolecarboxylates
Lee, Len F.,Schleppnik, Francis M.,Howe, Robert K.
, p. 1621 - 1630 (2007/10/02)
A variety of 2-halo-5-thiazolecarboxylates was prepared from substituted-3-aminoacrylates and 3-ketoesters.Selective reduction of 2-chloro-5-thiazolecarboxylates 4a, 4i and 4j with sodium borohydride in ethanol provided the corresponding 2-halo-5-thiazolemethanols 27 - 29.Nucleophilic displacement on methyl methanesulfonate (32c) occured selectivity at the 5-substituent to provide 2-chloro-4-(trifluoromethyl)-5-(heteroatom-substituted methyl)thiazoles 32d-f.
