16931-47-8 Usage
General Description
2-{[Methyl(phenyl)amino]carbonyl}benzoic acid is a compound with the chemical formula C15H13NO3. It is a derivative of benzoic acid and contains a carbonyl group attached to a methyl(phenyl)amino moiety. 2-{[METHYL(PHENYL)AMINO]CARBONYL}BENZOIC ACID is used in the pharmaceutical industry as an intermediate in the synthesis of various drugs and active pharmaceutical ingredients. It is also used in organic synthesis and chemical research as a building block for creating more complex molecules. The compound has potential applications in medicinal chemistry and drug development due to its structural features and reactivity. Overall, 2-{[Methyl(phenyl)amino]carbonyl}benzoic acid is a versatile chemical that has important roles in various fields, particularly in the development of pharmaceuticals and other biologically active compounds.
Check Digit Verification of cas no
The CAS Registry Mumber 16931-47-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,9,3 and 1 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 16931-47:
(7*1)+(6*6)+(5*9)+(4*3)+(3*1)+(2*4)+(1*7)=118
118 % 10 = 8
So 16931-47-8 is a valid CAS Registry Number.
InChI:InChI=1/C15H13NO3/c1-16(11-7-3-2-4-8-11)14(17)12-9-5-6-10-13(12)15(18)19/h2-10H,1H3,(H,18,19)
16931-47-8Relevant academic research and scientific papers
Siddiqui, Asher M.,Khalid, Anam,Khan, Arif,Azad, Chandra S.,Samim, Mohd.,Khan, Imran A.
, p. 4281 - 4287 (2020)
A novel methodology for the construction of various secondary (4 examples), tertiary amides (31 examples), and imides (16 examples) by a Cobalt(II) catalyzed oxidative amide coupling in aqueous media. The Co(III)-TMC was reacted with N-Heteroatom Carbene to form active catalyst Co(II)NHC-TMC in situ which involves in the coordination with Breslow's intermediate and SET for the activation of aldehyde and amides. The mechanism for activation of amide and amine differs on the basis of SET based nucleophilic addition and ligand exchange respectively. The regeneration of the catalyst was achieved using Fe(III)(EDTA)-H2O2 as oxidant. The use of Co(II)TMC-O2 was also found equally efficient in the process. The method is found regioselective for N?H activation in the presence of equally susceptible ortho-C?H bond activation. And amines were found more susceptible then the corresponding amide for the reaction.
