160171-18-6

Basic information

• Product Name: 3,5-dichloro-N-(1-chloro-3-methyl-2-oxo-pentan-3-yl)-4-methyl-benzamide
• Synonyms: 3,5-Dichloro-N-(3-chloro-1-ethyl-1-methyl-2-oxopropyl)-p-toluamide;Hsdb 7278;Zoxium;Zoxium 80W agricultral fungicide;3,5-dichloro-N-(1-chloro-3-methyl-2-oxo-pentan-3-yl)-4-methyl-benzamide;3,5-Dichloro-N-(3-chloro-1-ethyl-1-methyl-2-oxopropyl)-4-methylbenzamide
• CAS NO: 160171-18-6
• Molecular Formula: C14H16Cl3NO2
• Molecular Weight: 0
• Mol File: 160171-18-6.mol
• Article Data: 11

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 3,5-dichloro-N-(1-chloro-3-methyl-2-oxo-pentan-3-yl)-4-methyl-benzamide(CAS DataBase Reference)
• NIST Chemistry Reference: 3,5-dichloro-N-(1-chloro-3-methyl-2-oxo-pentan-3-yl)-4-methyl-benzamide(160171-18-6)
• EPA Substance Registry System: 3,5-dichloro-N-(1-chloro-3-methyl-2-oxo-pentan-3-yl)-4-methyl-benzamide(160171-18-6)

Safety Data

• Hazardous Substances Data: 160171-18-6(Hazardous Substances Data)

Usage

InChI:InChI=1/C14H16Cl3NO2/c1-4-14(3,12(19)7-15)18-13(20)9-5-10(16)8(2)11(17)6-9/h5-6H,4,7H2,1-3H3,(H,18,20)

Upstream product

• 113485-46-4 3,5-dichloro-4-methylbenzoyl chloride 
• 156052-68-5 zoxamide 
• 118725-00-1 methyl (R)-2-amino-2-methyl-butyrate hydrochloride 
• 3059-97-0 (2R)-2-amino-2-methylbutanoic acid 
• 92760-72-0 L-isovalin methyl ester hydrochloride 
• 595-40-4 L-isovaline 
• 39652-34-1 3,5-dichloro-4-methylbenzoic acid 
• 209809-70-1 2-(3,5-dichloro-4-methylphenyl)-4-ethyl-4-methyl-5-methyleneoxazoline 
• 87-90-1 trichloroisocyanuric acid 

Relevant articles and documents

Method for preparing benzamide compound

The invention provides a method for preparing a benzamide compound, and belongs to the technical field of organic synthesis. The method for preparing a benzamide compound provided by the invention comprises the following steps: mixing aryl-substituted dihydrooxazole, an acidic catalyst, water and a reaction solvent, and carrying out hydrolysis ring-opening reaction to obtain the benzamide compound, wherein the acidic catalyst is p-toluenesulfonic acid or sulfonic acid ion exchange resin. According to the invention, p-toluenesulfonic acid or sulfonic acid ion exchange resin is used as an acidiccatalyst, under the catalytic action of the p-toluenesulfonic acid or sulfonic acid ion exchange resin, aryl-substituted dihydrooxazole is subjected to hydrolysis ring-opening reaction to obtain thebenzamide compound, only metered toluenesulfonic acid or sulfonic acid ion exchange resin needs to be catalyzed, the toluenesulfonic acid or sulfonic acid ion exchange resin is convenient to remove after the reaction is completed, almost no waste is generated, and industrial production is convenient to achieve.

Enantiomer mixture and preparation method and application thereof

The invention provides an enantiomer mixture and a preparation method and application thereof, and belongs to the technical field of pesticide chemistry and organic synthesis. The enantiomer mixture is a mixture of S-zoxamide and R-zoxamide, and the enant

Process for the manufacture of acetonylbenzamides

Novel routes for the preparation of acetonylbenzamides are provided by the reaction of an amine and acyl chloride. Novel routes to various intermediates used in the manufacture of acetonylbenzamides are also disclosed.