40501-36-8

Basic information

• Product Name: 2-PHENOXYBENZOYL CHLORIDE
• Synonyms: 2-PHENOXYBENZOYL CHLORIDE;2-Phenoxybenzoyl chloride 90%;2-(Chlorocarbonyl)diphenyl ether;2-(Chlorocarbonyl)diphenyl ether, 2-(Chloroformyl)diphenyl ether;2-Phenoxybenzoylchloride90%
• CAS NO: 40501-36-8
• Molecular Formula: C₁₃H₉ClO₂
• Molecular Weight: 232.66
• Mol File: 40501-36-8.mol
• Article Data: 5

Chemical Properties

• Melting Point: 37 °C
• Boiling Point: 319.149 °C at 760 mmHg
• Flash Point: 118.552 °C
• Appearance: /
• Density: 1.248 g/cm³
• Vapor Pressure: 0mmHg at 25°C
• Refractive Index: 1.59
• CAS DataBase Reference: 2-PHENOXYBENZOYL CHLORIDE(CAS DataBase Reference)
• NIST Chemistry Reference: 2-PHENOXYBENZOYL CHLORIDE(40501-36-8)
• EPA Substance Registry System: 2-PHENOXYBENZOYL CHLORIDE(40501-36-8)

Safety Data

• Hazard Codes: C
• Hazardous Substances Data: 40501-36-8(Hazardous Substances Data)

Usage

General Description

2-Phenoxybenzoyl chloride is a chemical compound that is typically used as an intermediate in the production of pharmaceuticals and agrochemicals. It is a benzoyl chloride derivative with a phenoxy group attached to the benzene ring, and it has a molecular formula of C13H9ClO2. 2-PHENOXYBENZOYL CHLORIDE is known for its reactivity and ability to undergo substitution reactions, making it useful in the synthesis of various organic compounds. It is also used as a building block in the preparation of dyes, perfumes, and other specialty chemicals. However, it should be handled with caution due to its corrosive and irritant properties.

InChI:InChI=1/C13H9ClO2/c14-13(15)11-8-4-5-9-12(11)16-10-6-2-1-3-7-10/h1-9H

Upstream product

• 88-67-5 2-Iodobenzoic acid 
• 2243-42-7 2-phenoxybenzoic acid 
• 19434-34-5 2-(phenoxy)benzaldehyde 
• 62256-41-1 2-(4-nitrophenoxy)benzaldehyde 
• 6476-32-0 o-phenoxybenzonitrile 
• 394-47-8 2-fluorobenzonitrile 

Downstream Products

• 143951-58-0 {(S)-1-[2-((3S,11bS)-9,10-Dimethoxy-1,3,4,6,7,11b-hexahydro-2H-pyrido[2,1-a]isoquinolin-3-yl)-ethyl]-6,7-dimethoxy-3,4-dihydro-1H-isoquinolin-2-yl}-(2-phenoxy-phenyl)-methanone 
• 143951-58-0 {(S)-1-[2-((3R,11bR)-9,10-Dimethoxy-1,3,4,6,7,11b-hexahydro-2H-pyrido[2,1-a]isoquinolin-3-yl)-ethyl]-6,7-dimethoxy-3,4-dihydro-1H-isoquinolin-2-yl}-(2-phenoxy-phenyl)-methanone 
• 143951-58-0 {(S)-1-[2-((3S,11bR)-9,10-Dimethoxy-1,3,4,6,7,11b-hexahydro-2H-pyrido[2,1-a]isoquinolin-3-yl)-ethyl]-6,7-dimethoxy-3,4-dihydro-1H-isoquinolin-2-yl}-(2-phenoxy-phenyl)-methanone 
• 143951-58-0 {(S)-1-[2-((3R,11bS)-9,10-Dimethoxy-1,3,4,6,7,11b-hexahydro-2H-pyrido[2,1-a]isoquinolin-3-yl)-ethyl]-6,7-dimethoxy-3,4-dihydro-1H-isoquinolin-2-yl}-(2-phenoxy-phenyl)-methanone 
• 90-47-1 xanth-9-one 
• 72084-13-0 2-phenoxybenzamide 
• 618430-03-8 3-methylsulfanyl-5-(2-phenoxy-phenyl)-4H-[1,2,4]triazole 
• 318730-26-6 (6R,7R)-7-Methoxy-3-(1-methyl-1H-tetrazol-5-ylsulfanylmethyl)-8-oxo-7-(2-phenoxy-benzoylamino)-5-oxa-1-aza-bicyclo[4.2.0]oct-2-ene-2-carboxylic acid 
• 318730-57-3 (6R,7R)-7-Methoxy-3-(1-methyl-1H-tetrazol-5-ylsulfanylmethyl)-8-oxo-7-(2-phenoxy-benzoylamino)-5-oxa-1-aza-bicyclo[4.2.0]oct-2-ene-2-carboxylic acid 4-benzhydryloxycarbonyl-benzyl ester 
• 892390-41-9 tert-butyl (3S)-3-[(cyclobutylmethyl)(2-phenoxybenzoyl)amino]pyrrolidine-1-carboxylate 
• 891944-52-8 tert-butyl (3S)-3-[(2,2-difluoropropyl)(2-phenoxybenzoyl)amino]pyrrolidine-1-carboxylate 
• 892390-54-4 tert-butyl (3S)-3-[ethyl(2-phenoxybenzoyl)amino]pyrrolidine-1-carboxylate 
• 177711-41-0 3-(2-phenoxybenzoyl)-1phenyl-imidazolidin-2,4-dione 

Relevant articles and documents

Formal Aniline Synthesis from Phenols through Deoxygenative N-Centered Radical Substitution

Phenolic, lignin-derived substrates have emerged as desirable biorenewable chemical feedstocks for coupling reactions. A radical-mediated conversion of phenol derivatives to anilines is reported, using unfunctionalized hydroxamic acids as the N-centered radical source. The applicability of this triethyl phosphite mediated O-atom transfer approach, which tolerates a range of steric and electronic demands to naturally occurring phenols and lignin models, has been demonstrated in this work to access the corresponding aniline derivatives.

SUBSTITUTED CYCLOHEXYL-1,4-DIAMINE DERIVATIVES WITH A CHAIN EXTENSION

The invention relates to substituted cyclohexyl-1,4-diamine derivatives, to a method for their production, to medicaments containing said compounds and to the use of substituted cyclohexyl-1,4-diamine derivatives for producing medicaments.

Process for producing α-ketoamide derivative

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