2447-96-3

Basic information

• Product Name: 4-Chloro-N-(3-chlorophenyl)benzaMide, 97%
• Synonyms: 4-Chloro-N-(3-chlorophenyl)benzaMide, 97%
• CAS NO: 2447-96-3
• Molecular Formula: C13H9Cl2NO
• Molecular Weight: 266.12266
• Mol File: 2447-96-3.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 315.1°C at 760 mmHg
• Flash Point: 144.4°C
• Appearance: /
• Density: 1.384g/cm³
• Vapor Pressure: 0.000447mmHg at 25°C
• Refractive Index: 1.656
• CAS DataBase Reference: 4-Chloro-N-(3-chlorophenyl)benzaMide, 97%(CAS DataBase Reference)
• NIST Chemistry Reference: 4-Chloro-N-(3-chlorophenyl)benzaMide, 97%(2447-96-3)
• EPA Substance Registry System: 4-Chloro-N-(3-chlorophenyl)benzaMide, 97%(2447-96-3)

Safety Data

• Hazardous Substances Data: 2447-96-3(Hazardous Substances Data)

Usage

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

Upstream product

• 14064-15-4 (4-chlorophenyl)trimethylstannane 
• 2909-38-8 m-chlorophenyl isocyanate 

Downstream Products

• 5892-89-7 (4-Chloro-benzoyl)-(3-chloro-phenyl)-carbamic acid isopropyl ester 

Relevant articles and documents

Facile and Effective Synthesis of Unusually Substituted Aromatic N-Phenylamides

A mild and effective new method for the preparation of a variety of arylamides 3a-i as well as heterocyclic 5a, b and 6 and olefinic amides 7, 9 is described.The reaction of trialkylstannyl-substituted aromatic, heterocyclic or vinylic hydrocarbons with aryl isocyanates in the presence of aluminium trichloride provides the corresponding N-aryl-substituted amides in good to excellent yields.The stannyl group serves as a powerful leaving group superior to hydrogen by several powers of ten which allows, via ipso substitution, to obtain isomer patterns not accessible by normal electrophilic substitution reactions, e. g. substitution in meta position with respect to a methoxy group.