77505-85-2 Usage
Uses
Used in Pharmaceutical Industry:
ETHYL 2-AMINO-5-PHENYL-4-THIAZOLECARBOXYLATE is used as a key component in drug creation for its bioactive properties. It is recognized for its potential in developing new medications.
Used in Antifungal Applications:
In the field of microbiology, ETHYL 2-AMINO-5-PHENYL-4-THIAZOLECARBOXYLATE is used as an antifungal agent, leveraging its ability to inhibit fungal growth and protect against fungal infections.
Used in Antitumor Applications:
ETHYL 2-AMINO-5-PHENYL-4-THIAZOLECARBOXYLATE is employed as an antitumor agent, contributing to the development of cancer treatments by targeting and inhibiting tumor growth.
Used in Antimicrobial Applications:
ETHYL 2-AMINO-5-PHENYL-4-THIAZOLECARBOXYLATE is also used as an antimicrobial agent, playing a role in the development of treatments to combat bacterial infections and other microorganisms.
Check Digit Verification of cas no
The CAS Registry Mumber 77505-85-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,5,0 and 5 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 77505-85:
(7*7)+(6*7)+(5*5)+(4*0)+(3*5)+(2*8)+(1*5)=152
152 % 10 = 2
So 77505-85-2 is a valid CAS Registry Number.
InChI:InChI=1/C12H12N2O2S/c1-2-16-11(15)9-10(17-12(13)14-9)8-6-4-3-5-7-8/h3-7H,2H2,1H3,(H2,13,14)
77505-85-2Relevant academic research and scientific papers
Synthesis of 2-amino-5-arylthiazoles by palladium-catalyzed arylation at the C5 position with aryl iodides
Priego, Julián,Gutiérrez, Sonia,Ferritto, Rafael,Broughton, Howard B.
, p. 2957 - 2960 (2008/03/12)
A new synthetic route to afford 2-amino-5-aryl thiazoles has been developed. The starting aminothiazole derivative can be arylated at position 5 with aryl iodides under palladium-catalyzed conditions. Mechanistic studies suggest a proton-abstraction pathw
Reaction of Dicyano Epoxides with Thiocyanate Ion: Route to α-Thiocyanato Derivatives or to 2-Acetylimino-1,3-oxathioles and X-Ray Crystal Structure of 2-Acetylimino-4-(4-tolyl)-1,3-oxathiole-5-carbonitrile
Marechal, Alenka Majcen Le,Robert, Albert,Leban, Ivan
, p. 351 - 356 (2007/10/02)
β-Aryl dicyano epoxides reacted as synthetic equivalents of ketene dications with KSCN in aq. dimethyl sulfoxide or EtOH, or with NH4SCN in acetonitrile, to give α-thiocyanato derivatives.When Ac2O was used as a solvent, the 1,3-oxathiolane intermediates
SYNTHESIS OF FUNCTIONALLY SUBSTITUTED 5-PHENYLTHIAZOLES
Mamedov, V. A.,Nuretdinov, I. A.,Sadkova, D. N.
, p. 2591 - 2593 (2007/10/02)
The reaction of esters and amides of 3-phenyl-3-chloro-2-oxopropionic acid with thioamides and thiourea gave new 5-phenylthiazoles.
