77711-35-4 Usage
General Description
Methyl 2-([(benzoylamino)carbothioyl]amino)benzenecarboxylate is a chemical compound with a complex molecular structure. It is a derivative of benzoic acid and contains the elements carbon, hydrogen, nitrogen, and oxygen. METHYL 2-([(BENZOYLAMINO)CARBOTHIOYL]AMINO)BENZENECARBOXYLATE is often used in organic synthesis and medicinal chemistry as a reagent or building block for the synthesis of various pharmaceutical and biologically active compounds. The presence of the carbothioyl and benzoylamino functional groups in its structure makes it suitable for a wide range of chemical reactions, making it a valuable intermediate in organic chemistry. Further research and studies on its properties and potential applications are ongoing.
Check Digit Verification of cas no
The CAS Registry Mumber 77711-35-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,7,1 and 1 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 77711-35:
(7*7)+(6*7)+(5*7)+(4*1)+(3*1)+(2*3)+(1*5)=144
144 % 10 = 4
So 77711-35-4 is a valid CAS Registry Number.
InChI:InChI=1/C16H14N2O3S/c1-21-15(20)12-9-5-6-10-13(12)17-16(22)18-14(19)11-7-3-2-4-8-11/h2-10H,1H3,(H2,17,18,19,22)
77711-35-4Relevant articles and documents
REACTIONS OF N-BENZOYL ISOTHIOCYANATE WITH ANTHRANILIC ACID AND METHYL ANTHRANILATE
Kavalek, Jaromir,Kotyk, Milan,El Bahaie, Said,Sterba, Vojeslav
, p. 246 - 255 (2007/10/02)
N-Benzoyl-N'-(2-carboxy- and -2-methoxycarbonylphenyl)thioureas have been obtained by the reaction of N-benzoyl isothiocyanate with anthranilic acid and methyl anthranilate, respectively.Kinetics of cyclization of these compounds into 2-mercapto-3,4-dihydro-4-quinazolone have been studied in water and in methanol.In the base-catalyzed cyclization of N-benzoyl-N'-(2-carboxyphenyl)thiourea the proper cyclization is preceded by solvolysis of the benzoyl group.In the case of N-benzoyl-N'-(2-methoxycarbonylphenyl)thiourea the reaction rate is limited by the base-catalyzed cyclization of the starting benzoyl derivative; the benzoyl group is split off in a subsequent rapid step.
