7508-77-2

Usage

Uses

Used in Pharmaceutical Industry:
2-Chloro-N-(4-Methoxyphenyl)benzaMide, 97% is used as an intermediate in the synthesis of pharmaceuticals for its potential therapeutic properties and contribution to the development of new drugs.
Used in Agrochemical Industry:
2-Chloro-N-(4-Methoxyphenyl)benzaMide, 97% is utilized as an intermediate in the production of agrochemicals, playing a role in the development of pesticides and other agricultural products to improve crop yield and protection.
Used in Dye and Pigment Production:
2-Chloro-N-(4-Methoxyphenyl)benzaMide, 97% is used in the creation of dyes and pigments for various applications, including textiles, plastics, and printing inks, due to its chemical structure that can contribute to color intensity and stability.

InChI:InChI=1/C14H12ClNO2/c1-18-11-8-6-10(7-9-11)16-14(17)12-4-2-3-5-13(12)15/h2-9H,1H3,(H,16,17)

Upstream product

• 118-91-2 ortho-chlorobenzoic acid 

Downstream Products

• 38088-96-9 2-methoxyphenanthridin-6(5H)-one 
• 1372788-44-7 C₁₅H₁₄ClNO₂ 
• 91233-33-9 3-phenylmethylene-2-(4-methoxyphenyl)isoindole-1-one 

Relevant academic research and scientific papers

Direct arylation under catalysis of an oxime-derived palladacycle: Search for a phosphane-free method

A phosphane-free method for the direct arylation of benzothiazole by employing oxime-derived palladacycle 1 as a catalyst was developed. The new catalyst system can be used for 2-arylations by using aryl bromides and iodides. In addition, this method is especially suitable for the intramolecular direct coupling of bromo-and iodoamides, as well aschloroamides, to achieve a rapid synthesis of benzo[c]phenanthridine alkaloids. Direct arylation reactions under catalysis of an oxime-derived palladacycle were investigated. This phosphane-free method is applicable for the 2-arylation of benzothiazole and is especially suitable for the intramolecular direct coupling of bromo-and iodoamides, as well as chloroamides, to achieve rapid synthesis of benzo[c]phenanthridine alkaloids. Copyright

Substituted 2-phenyl-4-quinolone-3-carboxylic acid compounds and their use as antitumor agents

Substituted 2-phenyl-4-quinolone-3-carboxylic acid derivatives and their salts were synthesized. The results of preliminary screening revealed that these compounds are potent in killing solid tumor cancers.