47030-01-3

Basic information

• Product Name: Benzeneacetic acid, a-phenyl-a-propoxy-
• CAS NO: 47030-01-3
• Molecular Formula: C17H18O3
• Molecular Weight: 270.328
• Mol File: 47030-01-3.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Benzeneacetic acid, a-phenyl-a-propoxy-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzeneacetic acid, a-phenyl-a-propoxy-(47030-01-3)
• EPA Substance Registry System: Benzeneacetic acid, a-phenyl-a-propoxy-(47030-01-3)

Safety Data

• Hazardous Substances Data: 47030-01-3(Hazardous Substances Data)

Upstream product

• 71-23-8 propan-1-ol 
• 7475-56-1 chloro(diphenyl)acetic acid 
• 2766-01-0 α.α-Diphenyl-α-propargyloxyessigsaeure 
• 56290-12-1 chloro-diphenyl-acetic acid propyl ester 
• 88857-84-5 N-(chloro-diphenyl-acetyl)-N'-methyl-urea 
• 54556-98-8 propiverine hydrochloride 
• 94686-44-9 diphenyl-propoxy-acetic acid propyl ester 

Downstream Products

• 87415-87-0 Diphenyl-propoxy-acetic acid 3-diethylamino-2-hydroxy-propyl ester; hydrochloride 
• 128887-47-8 Diphenyl-propoxy-acetic acid 3-azepan-1-yl-propyl ester 
• 102752-75-0 diphenyl-propoxy-acetic acid-(2-diethylamino-ethyl ester) 

Relevant articles and documents

Raney nickel-catalyzed hydrogenation of unsaturated carboxylic acids with sodium borohydride in water

A mild, selective, and green method for the reduction of unsaturated carboxylic acids with sodium borohydride-Raney nickel (W6) system in water is reported. This method is practical and safe and avoids use of organic solvents. Taylor & Francis Group, LLC.

Biomimetic oxidation of propiverinhydrochloride and 1-methyl-4-piperidyl benzilate

The reaction of propiverinhydrochloride (1) and 1-methyl-4-piperidyl benzilate (2) with the biomimetic system manganese(III)-5,10,15,20-tetrakis(pentafluorophenyl)porphyrin chloride (MnTPFPPCl)/pyridine/hydrogen peroxide affords unchanged 1 and 2 and 15 potential metabolites, which were isolated and identified. These compounds are products of cleavage of the ester bond, of O-dealkylation, aromatic oxidation, respectively of decarboxylation, demethylation, and N-oxidation. Products were identified by TLC, UV, and MS in comparison with authentic samples. Thereby we found a nearly conformity with rat metabolism.