166670-25-3

Basic information

• Product Name: 3,4-Dimethoxy-benzalanilin
• Synonyms: 3,4-Dimethoxy-benzalanilin
• CAS NO: 166670-25-3
• Molecular Weight: 241.29
• Mol File: 166670-25-3.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 3,4-Dimethoxy-benzalanilin(CAS DataBase Reference)
• NIST Chemistry Reference: 3,4-Dimethoxy-benzalanilin(166670-25-3)
• EPA Substance Registry System: 3,4-Dimethoxy-benzalanilin(166670-25-3)

Safety Data

• Hazardous Substances Data: 166670-25-3(Hazardous Substances Data)

Upstream product

• 64-10-8 phenyl carbamate 
• 144017-75-4 3-(3,5-dimethoxyphenyl)-1-phenylprop-2-en-1-one 
• 7311-34-4 3,5-dimethoxybenzaldehdye 
• 62-53-3 aniline 

Downstream Products

• 166670-12-8 [Pd(C₆H₂(OCH₃)2CHNC₆H₅)(CH₃CO₂)]2 
• 592-42-7 1,5-Hexadien 

Relevant articles and documents

A concise route to biaryls: Formal synthesis of biaryl diamino diacid (AB segment) of vancomycin

An efficient approach to the AB segment of vancomycin involving triphenylphosphine-catalysed coupling of the substituted aryl lithio compound (13) with palladium complex (14) of aromatic Schiff base derived from 3,5- dimethoxybenzaldehyde is described.

Base-catalyzed synthesis of amides and imines via C-C and CC bond cleavage

A transition metal free base catalyzed approach for C-N bond formation via C-C and CC bond activation has been developed. The N-arylureas reacted smoothly with 1,3-dicarbonyls and α,β-unsaturated ketones to furnish the corresponding amides and imines respectively in moderate to excellent yields.