137374-28-8

Basic information

• Product Name: N-Benzyl-4-chloro-N-MethylbenzaMide, 97%
• Synonyms: N-Benzyl-4-chloro-N-MethylbenzaMide, 97%
• CAS NO: 137374-28-8
• Molecular Formula: C₁₅H₁₄ClNO
• Molecular Weight: 259.73076
• Mol File: 137374-28-8.mol
• Article Data: 12

Chemical Properties

• Appearance: /
• CAS DataBase Reference: N-Benzyl-4-chloro-N-MethylbenzaMide, 97%(CAS DataBase Reference)
• NIST Chemistry Reference: N-Benzyl-4-chloro-N-MethylbenzaMide, 97%(137374-28-8)
• EPA Substance Registry System: N-Benzyl-4-chloro-N-MethylbenzaMide, 97%(137374-28-8)

Safety Data

• Hazardous Substances Data: 137374-28-8(Hazardous Substances Data)

Upstream product

• 81616-14-0 tert-butyl N-benzyl-N-methylcarbamate 
• 100-46-9 benzylamine 
• 201230-82-2 carbon monoxide 
• 1679-18-1 4-Chlorophenylboronic acid 
• 103-67-3 benzyl-methyl-amine 
• 3555-71-3 N-benzyl-N-chloromethylamine 
• 104-88-1 4-chlorobenzaldehyde 
• 1126-46-1 Methyl 4-chlorobenzoate 
• 26163-40-6 N-(4-chlorobenzoyl)piperidine 

Downstream Products

• 26163-40-6 N-(4-chlorobenzoyl)piperidine 

Relevant articles and documents

Visible-Light-Mediated Oxidative Amidation of Aldehydes by Using Magnetic CdS Quantum Dots as a Photocatalyst

A magnetic CdS quantum dot (Fe3O4/polydopamine (PDA)/CdS) was synthesized through a facile and convenient method from inexpensive starting materials. Characterization of the prepared catalyst was performed by means of FTIR spectrosco

Amidation of unactivated ester derivatives mediated by trifluoroethanol

A catalytic amidation protocol mediated by 2,2,2-trifluoroethanol has been developed, facilitating the condensation of unactivated esters and amines, furnishing both secondary and tertiary amides. The complete scope and limitations of the method are described, along with modified conditions for challenging substrates such as acyclic secondary amines and chiral esters with retention of chiral integrity.

Radical-Induced Metal and Solvent-Free Cross-Coupling Using TBAI-TBHP: Oxidative Amidation of Aldehydes and Alcohols with N-Chloramines via C-H Activation

A solvent-free cross-coupling method for oxidative amidation of aldehydes and alcohols via a metal-free radial pathway has been demonstrated. The proposed methodology uses the TBAI-TBHP combination which efficiently induces metal-free C-H activation of aldehydes under neat conditions at 50 °C or ball-milling conditions at room temperature.