736994-63-1

Basic information

• Product Name: 3-bromo-1-(3-chloropyridin-2-yl)-N-[4-cyano-2-methyl-6-(methylcarbamoyl)phenyl]-1H-pyrazole-5-carboxamide
• Synonyms: cyantraniliprole; DPX-HGW86; HGW-86
• CAS NO: 736994-63-1
• Molecular Formula: C₁₉H₁₄BrClN₆O₂
• Molecular Weight: 473.7105
• Mol File: 736994-63-1.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 561.256°C at 760 mmHg
• Flash Point: 293.237°C
• Density: 1.612g/cm³
• Vapor Pressure: 0mmHg at 25°C
• Refractive Index: 1.704
• CAS DataBase Reference: 3-bromo-1-(3-chloropyridin-2-yl)-N-[4-cyano-2-methyl-6-(methylcarbamoyl)phenyl]-1H-pyrazole-5-carboxamide(CAS DataBase Reference)
• NIST Chemistry Reference: 3-bromo-1-(3-chloropyridin-2-yl)-N-[4-cyano-2-methyl-6-(methylcarbamoyl)phenyl]-1H-pyrazole-5-carboxamide(736994-63-1)
• EPA Substance Registry System: 3-bromo-1-(3-chloropyridin-2-yl)-N-[4-cyano-2-methyl-6-(methylcarbamoyl)phenyl]-1H-pyrazole-5-carboxamide(736994-63-1)

Safety Data

• Hazardous Substances Data: 736994-63-1(Hazardous Substances Data)

Upstream product

• 500011-86-9 3-bromo-1-(3-chloro-2-pyridinyl)-1H-pyrazole-5-carboxylic acid 
• 871239-18-8 2-amino-5-cyano-3-methyl-benzoic acid 

Relevant articles and documents

SOLID FORMS OF CYANTRANILIPROLE

Solid state forms of Cyantraniliprole, processes for preparation and agrochemical compositions thereof.

Method for preparing benzamide compound by using pressure reducing method

The invention relates to a method for preparing a benzamide compound represented by a general formula (I), wherein the reaction formula is defined in the specification, and each group in the formula is defined in the specification. According to the method, 3-bromo-1-(substituted pyridyl)-4,5-dihydro-1H-pyrazole-5-carboxylic acid (IV) is used as a raw material, and is simultaneously subjected to acyl chlorination and oxidation under a pressure reducing condition to prepare acyl chloride represented by a general formula (III), and the benzamide compound represented by the general formula (I) isprepared from the acyl chloride (III) and substituted aniline (II) in the absence of an acid-binding agent in a high yield manner.