55810-66-7

Basic information

• Product Name: Benzoyl chloride, 2-(phenylmethyl)-
• CAS NO: 55810-66-7
• Molecular Formula: C14H11ClO
• Molecular Weight: 230.694
• Mol File: 55810-66-7.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: Benzoyl chloride, 2-(phenylmethyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzoyl chloride, 2-(phenylmethyl)-(55810-66-7)
• EPA Substance Registry System: Benzoyl chloride, 2-(phenylmethyl)-(55810-66-7)

Safety Data

• Hazardous Substances Data: 55810-66-7(Hazardous Substances Data)

Upstream product

• 23450-18-2 2-benzyl-1-bromobenzene 
• 59142-47-1 (2-bromophenyl)phenylmethanol 
• 6630-33-7 ortho-bromobenzaldehyde 
• 108-86-1 bromobenzene 
• 612-35-1 2-Benzylbenzoic acid 
• 68-12-2 N,N-dimethyl-formamide 

Downstream Products

• 80239-71-0 2-Benzyl-benzoic acid 1-methyl-piperidin-4-yl ester; hydrochloride 
• 78987-17-4 2-Benzyl-N-o-tolyl-benzamide 
• 933987-20-3 methyl 3-(2-benzylphenyl)-2-diazo-3-oxopropanoate 
• 909787-58-2 3-methyl-benzoic acid N'-(2-benzyl-benzoyl)-hydrazide 
• 180340-11-8 methyl 4-[[(2-phenylmethyl)benzoyl]amino]-3-methoxybenzoate 
• 120935-81-1 1-<2-(phenylmethyl)benzoyl>-1,3-butanedione 
• 208175-54-6 (S)-2-Benzyl-N-(3-phenylpropan-1-ol-2-yl)benzamide 
• 1111702-44-3 2-benzyl-N-(4,4-diethoxybutyl)benzamide 
• 1456693-84-7 3-hydroxy-2-methoxy-3-phenylisoindolin-1-one 
• 6621-97-2 3-hydroxy-2,3-diphenyl-1-isoindolinone 
• 37019-94-6 2-(4-bromophenyl)-3-hydroxy-3-phenylisoindolin-1-one 
• 3532-71-6 3-hydroxy-3-phenyl-2-(p-tolyl)-2,3-dihydro-1H-inden-1-one 
• 17416-52-3 2-benzyl-3-hydroxy-3-phenyl-2,3-dihydroisoindol-1-one 
• 3593-38-2 2-cyclohexyl-3-hydroxy-3-phenylisoindolin-1-one 

Relevant articles and documents

Eosin Y as a Redox Catalyst and Photosensitizer for Sequential Benzylic C?H Amination and Oxidation

A new synergistic multicatalytic activation mode of eosin Y has been discovered by exploiting the redox potential of its ground state and excited state. This catalytic strategy proves to be an enabling tool for visible-light-driven sequential benzylic C?H amination and oxidation of o-benzyl-N-methoxyl-benzamides when using Selectfluor as a hydrogen atom transfer (HAT) reagent and O2 as oxidant. Efficient synthesis of a range of diversely functionalized 3-hydroxyisoindolinones can thus be achieved with good yields and selectivity at mild reaction conditions. Preliminary mechanistic studies and DFT calculations suggest that eosin Y works as a redox catalyst and photosensitizer.