4934-55-8

Basic information

• Product Name: 4-Amino-3-methylbenzophenone
• Synonyms: 4-Amino-3-methylbenzophenone
• CAS NO: 4934-55-8
• Molecular Formula: C₁₄H₁₃NO
• Molecular Weight: 211.26
• Mol File: 4934-55-8.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 395.7°C at 760 mmHg
• Flash Point: 193.1°C
• Appearance: /
• Density: 1.135g/cm³
• Vapor Pressure: 1.81E-06mmHg at 25°C
• Refractive Index: 1.616
• CAS DataBase Reference: 4-Amino-3-methylbenzophenone(CAS DataBase Reference)
• NIST Chemistry Reference: 4-Amino-3-methylbenzophenone(4934-55-8)
• EPA Substance Registry System: 4-Amino-3-methylbenzophenone(4934-55-8)

Safety Data

• Hazardous Substances Data: 4934-55-8(Hazardous Substances Data)

Usage

InChI:InChI=1/C14H13NO/c1-10-9-12(7-8-13(10)15)14(16)11-5-3-2-4-6-11/h2-9H,15H2,1H3

Upstream product

• 98-88-4 benzoyl chloride 
• 95-53-4 o-toluidine 
• 100-51-6 benzyl alcohol 
• 62441-37-6 4-benzyl-2-methylbenzenamine 
• 3113-71-1 3-methyl-4-nitrobenzoic acid 
• 584-70-3 N-benzoyl-2-methylaniline 

Downstream Products

• 31720-12-4 (4-benzoyl-2-methyl-phenyl)-carbamic acid ethyl ester 
• 855628-44-3 (8-methyl-[6]quinolyl)-phenyl ketone 
• 31720-23-7 4-Benzoyl-N-(4-benzoyl-2-methyl-phenyl)-benzamide 
• 31720-29-3 N-(4-benzoyl-2-methyl-phenyl)-2-(3-oxo-morpholin-4-yl)-acetamide 
• 31720-30-6 N-(4-benzoyl-2-methyl-phenyl)-2-morpholin-4-yl-acetamide 
• 71968-97-3 C₂₈H₂₅ClN₄ 
• 31684-60-3 (E)-4-(4-Benzoyl-2-methyl-phenylamino)-pent-2-enoic acid ethyl ester 
• 31720-22-6 Acetic acid 2-[(4-benzoyl-2-methyl-phenylcarbamoyl)-methoxy]-ethyl ester 
• 71961-33-6 C₂₈H₂₆N₄ 
• 31720-15-7 N-(4-Benzoyl-2-methyl-phenyl)-2,2-dimethyl-propionamide 
• 71968-77-9 C₂₇H₂₄N₄ 
• 31720-13-5 (E)-But-2-enoic acid (4-benzoyl-2-methyl-phenyl)-amide 
• 31720-14-6 N-(4-Benzoyl-2-methyl-phenyl)-butyramide 
• 146470-25-9 C₁₅H₁₇N₅*2ClH 

Relevant articles and documents

Coumarin-surfactant modified polyoxometalate catalyzed cross dehydrogenative coupling of benzyl alcohol with the: Para -C-H of unprotected aniline

This paper presents a novel method for synthesizing para-aminobenzophenone and its derivatives (p-ABPs) using a coumarin-surfactant modified polyoxometalate as the catalyst. Preliminary mechanistic studies indicate that the reaction has undergone an oxidative cross dehydrogenative coupling process. This method has the advantages of an easy process, a convenient raw material source, safe and green oxidants, and tolerances of several functional groups.

Ecofriendly solvent free microwave enhanced thermal Fries rearrangement of anilides and phenyl ureas

A rapid, cleaner, cost effective and ecofriendly synthesis of exclusive para aminoaryl ketones and para aminoaryl amides in solvent free conditions using solid supports under microwave irradiation is achieved.