1218923-24-0

Basic information

• Product Name: 2-(3-(N-benzotriazolcarbonyloxy)(phenyl)(methyl)phenyl) propanoic acid benzotriazolide
• Synonyms: 2-(3-(N-benzotriazolcarbonyloxy)(phenyl)(methyl)phenyl) propanoic acid benzotriazolide
• CAS NO: 1218923-24-0
• Molecular Weight: 502.532
• Mol File: 1218923-24-0.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 2-(3-(N-benzotriazolcarbonyloxy)(phenyl)(methyl)phenyl) propanoic acid benzotriazolide(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(3-(N-benzotriazolcarbonyloxy)(phenyl)(methyl)phenyl) propanoic acid benzotriazolide(1218923-24-0)
• EPA Substance Registry System: 2-(3-(N-benzotriazolcarbonyloxy)(phenyl)(methyl)phenyl) propanoic acid benzotriazolide(1218923-24-0)

Safety Data

• Hazardous Substances Data: 1218923-24-0(Hazardous Substances Data)

Upstream product

• 22071-15-4 ketoprofen 
• 59960-32-6 Dihydroketoprofen 
• 65095-13-8 1-benzotriazolecarboxylic acid chloride 

Downstream Products

• 1218923-34-2 (3-(1-oxo-1-(pyrrolidin-1-yl)propan-2-yl)phenyl)(phenyl)methyl pyrrolidine-1-carboxylate 
• 1218923-35-3 (3-(1-oxo-1-(piperidin-1-yl)propan-2-yl)phenyl)(phenyl)methyl piperidine-1-carboxylate 
• 1218923-25-1 (3-(1-(methoxycarbamoyl)ethyl)phenyl)(phenyl)methyl methoxycarbamate 
• 1218923-26-2 (3-(1-(ethoxycarbamoyl)ethyl)phenyl)(phenyl)methyl ethoxycarbamate 
• 1218923-30-8 (3-(1-(cyclohexylcarbamoyl)ethyl)phenyl)(phenyl)methyl cyclohexylcarbamate 
• 1218923-33-1 (3-(1-((2-phenylethyl)carbamoyl)ethyl)phenyl)(phenyl)methyl (2-phenylethyl)carbamate 
• 1218923-28-4 (3-(1-(cyclopentylcarbamoyl)ethyl)phenyl)(phenyl)methyl cyclopentylcarbamate 
• 1218923-31-9 (3-(1-(cyclohexanemethylcarbamoyl)ethyl)phenyl)(phenyl)methyl cyclohexanemethylcarbamate 

Relevant articles and documents

The novel amidocarbamate derivatives of ketoprofen: Synthesis and biological activity

A series of novel ketoprofen derivatives 4a-j bearing both amide and carbamate functionalities were prepared using the benzotriazole method of carboxylic and hydroxy group activation. Selective reduction of ketoprofen produced hydroxy derivative 2, which