31802-10-5

Basic information

• Product Name: (2-benzoylphenyl)(morpholin-4-yl)methanone
• Synonyms: (2-Benzoylphenyl)(morpholin-4-yl)methanone; (2-Benzoyl-phenyl)-morpholin-4-yl-methanone; methanone, (2-benzoylphenyl)-4-morpholinyl-
• CAS NO: 31802-10-5
• Molecular Formula: C₁₈H₁₇NO₃
• Molecular Weight: 295.3325
• Mol File: 31802-10-5.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 521°C at 760 mmHg
• Flash Point: 268.9°C
• Density: 1.211g/cm³
• Vapor Pressure: 5.9E-11mmHg at 25°C
• Refractive Index: 1.597
• CAS DataBase Reference: (2-benzoylphenyl)(morpholin-4-yl)methanone(CAS DataBase Reference)
• NIST Chemistry Reference: (2-benzoylphenyl)(morpholin-4-yl)methanone(31802-10-5)
• EPA Substance Registry System: (2-benzoylphenyl)(morpholin-4-yl)methanone(31802-10-5)

Safety Data

• Hazardous Substances Data: 31802-10-5(Hazardous Substances Data)

Upstream product

• 110-91-8 morpholine 
• 18852-53-4 3-chloro-3-phenylphthalide 
• 85-52-9 2-Benzoylbenzoic acid 
• 1468-28-6 4-benzoylmorpholine 
• 100-52-7 benzaldehyde 

Downstream Products

• 24088-70-8 (2-morpholin-4-ylmethyl-phenyl)-phenyl-methanol 

Relevant articles and documents

Rhodium-catalyzed oxidative ortho -acylation of benzamides with aldehydes: Direct functionalization of the sp2 C-H bond

A rhodium-catalyzed oxidative acylation of benzamides with aryl aldehydes via direct sp2 C-H bond cleavage is described. In the presence of [Cp*RhCl2]2, AgSbF6, and silver carbonate as an oxidant, N,N-diethyl be

Effect of Nucleophilicity and Leaving Group Ability on the SN2 Reactions of Amines with (Acyloxy)alkyl α-Halides: A Product Distribution Study

The course of the reaction of amines with (acyloxy)alkyl α-halides has been found to depend on the nucleophilicity of the amines and the leaving group ability of the halides.More nucleophilic amines tended to give acylated products 2 from the reaction while less nucleophilic amines gave alkylated products 3.The use of a better leaving group also tended to favor the formation of a greater amount of alkylated product.These results have been compared to the observations of Westaway on the effect of leaving group ability and nucleophilicity on the bond lengths in the transit ion state of SN2 reactions.In addition, secondary amines have been shown to cause the rearrangement of 2-formylbenzamides to 3-amino-1(3H)-isobenzofuranones.