40501-36-8

Usage

Uses

Used in Pharmaceutical Industry:
2-Phenoxybenzoyl chloride is used as a chemical intermediate for the synthesis of various pharmaceuticals, contributing to the development of new drugs and medications.
Used in Agrochemical Industry:
In the agrochemical sector, 2-Phenoxybenzoyl chloride is utilized as a precursor in the production of agrochemicals, aiding in the creation of pesticides and other agricultural products.
Used in Organic Synthesis:
2-Phenoxybenzoyl chloride is employed as a reactive intermediate in organic synthesis, enabling the formation of a wide range of organic compounds through substitution reactions.
Used in Dye and Perfume Production:
As a building block, 2-Phenoxybenzoyl chloride is used in the preparation of dyes and perfumes, contributing to the color and fragrance of various consumer products.
Used in Specialty Chemicals:
2-Phenoxybenzoyl chloride is also utilized in the production of specialty chemicals, where its unique properties are harnessed for specific applications in industries such as plastics, coatings, and textiles.

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

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

Downstream Products

• 64506-89-4 β-{4-[2-(2-phenoxybenzamido)-ethyl]-phenyl}-propionic acid 
• 136955-06-1 2-Phenoxy-benzoic acid (1R,3R,5S)-8-methyl-8-aza-bicyclo[3.2.1]oct-3-yl ester 
• 618429-99-5 5-(2-phenoxyphenyl)-2H-1,2,4-triazole-3(4H)-thione 
• 92103-14-5 ω-Chlor-2-phenoxy-acetophenon 
• 2243-42-7 2-phenoxybenzoic acid 
• 313347-52-3 N₁-[4-(4-Amino-1H-imidazo[4,5-c]quinolin-1-yl)butyl]-2-phenoxybenzamide 
• 120041-60-3 2,N-Diphenoxy-benzamide 
• 76279-46-4 N-methoxy-N-methyl-2-phenoxybenzamide 

Relevant academic research and scientific papers

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.

Electrochemical Reductive Smiles Rearrangement for C-N Bond Formation

A conceptually new and synthetically valuable radical Smiles rearrangement reaction is reported under undivided electrolytic conditions. This protocol employs an entirely new strategy for the electrochemical radical Smiles rearrangement. Remarkably, an amidyl radical generated from the cleavage of the N-O bond under reductive electrolytic conditions plays a crucial role in this transformation. Various hydroxylamine derivatives bearing different substituents are suitable in this electrochemical transformation, furnishing the corresponding amides in up to 86% yield.

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.

Inhibitors of microsomal triglyceride transfer protein and method

Compounds are provided which inhibit microsomal triglyceride transfer protein and thus are useful for lowering serum lipids and treating atherosclerosis and related diseases. The compounds have the structure STR1 wherein R1 to R6, Q,

Process for producing α-ketoamide derivative

There is disclosed an efficient process for producing α-ketoacetamide of the formula: STR1 which is useful as an intermediate for the production of various alkoxyiminoacetamide compounds to be used for agricultural fungicides. In this process, a correspon