2670-39-5

Usage

Uses

Used in Pharmaceutical Industry:
2-Chloro-N-(2-chlorophenyl)benzamide, 97% is used as an intermediate in the synthesis of pharmaceuticals for its ability to be incorporated into the molecular structure of various drugs.
Used in Agrochemical Industry:
2-Chloro-N-(2-chlorophenyl)benzamide, 97% is used as an intermediate in the synthesis of agrochemicals for its potential to be utilized in the development of pesticides and other agricultural products.
Used in Dye and Pigment Production:
2-Chloro-N-(2-chlorophenyl)benzamide, 97% is used in the production of dyes and pigments due to its chemical properties that can contribute to the color and stability of these products.
Used in Organic Compound Manufacturing:
2-Chloro-N-(2-chlorophenyl)benzamide, 97% is used in the manufacturing of other organic compounds for its potential to be a building block in the creation of various organic molecules for different applications.
Its high purity of 97% makes 2-Chloro-N-(2-chlorophenyl)benzamide suitable for use in precise and sensitive chemical reactions and processes across these industries.

InChI:InChI=1/C13H9Cl2NO/c14-10-6-2-1-5-9(10)13(17)16-12-8-4-3-7-11(12)15/h1-8H,(H,16,17)

Upstream product

• 609-65-4 o-chlorobenzoyl chloride 
• 95-51-2 o-chloroaniline 
• 118-91-2 ortho-chlorobenzoic acid 

Downstream Products

• 93-98-1 N-phenyl benzoyl amide 
• 33238-21-0 3-benzylidene-2-(2-chlorophenyl)isoindole-1-one 

Relevant academic research and scientific papers

Continuous flow photochemistry as an enabling synthetic technology: Synthesis of substituted-6(5: H)-phenanthridinones for use as poly(ADP-ribose) polymerase inhibitors

Methods utilizing continuous flow photochemistry, an enabling synthetic technology, have been developed for the generation of phenanthridinones via an intramolecular photochemical cyclization of 2-chlorobenzamides for the purposes of generating poly(ADP-ribose) polymerase inhibitors. Herein we report 16 examples of a single-step flow photocyclization which produces substituted phenanthridinones in yields up to 99%, while a two-step method leads directly to phenanthridinones from 2-chlorobenzoyl chlorides and anilines via a novel continuous flow amidation/photocyclization protocol. Overall, the flow photocyclization reactions typically progress in good to excellent yields, and in a superior fashion to analogous batch methods, greatly enabling the drug discovery process.

Synthesis and biological evaluation of a series of 2-(Substitutedphenyl) benzothiazoles

A series of 2-phenylbenzothiazoles has been synthesized either by i) condensation of different aromatic aldehydes with 2-aminothiophenol or ii) condensation of N-(2-chlorophenyl)benzothioamides in KOH catalyzed by potassium fericyanide. The structures of

Infrared spectra of N-aryl substituted amides 2/4-XC6H 4NHCOR (R = H, CH3-iXi, C6H 5 or C6H5Cl; X = H, Cl or CH3 and i = 0, 1, 2 or 3)

Several N-(aryl)-substituted amides of the general formula, 2/4-XC 6H4NHCOR (where X = H, Cl or CH3 and R = H, CH3, CH2CH3, CH(CH3)2, C(CH3)3, C6H5 or C6H 5Cl) are prepared, characterised and their infrared spectra measured in the solid state and analysed. Generally chloro substitution in the side chain increases the C=O absorptions, while that of methyl groups lower the wave numbers. Amides with trimethyl substituted side chains absorb at higher wavenumbers. But the N-H and C-N stretching vibrations do not show particular trends on side chain substitution. This may be due to the fact that the spectra were recorded in the solid state and the compounds may crystallise in different forms in the solid state. The intercorrelations of C=O and N-H absorption frequencies of all the amides have been made. The correlations are reasonably linear with some exceptions for the reasons stated above.