859103-01-8

Basic information

• Product Name: (3,5-di-benzyloxy)-N,N-diethylbenzamide
• Synonyms: (3,5-di-benzyloxy)-N,N-diethylbenzamide
• CAS NO: 859103-01-8
• Molecular Weight: 389.494
• Mol File: 859103-01-8.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: (3,5-di-benzyloxy)-N,N-diethylbenzamide(CAS DataBase Reference)
• NIST Chemistry Reference: (3,5-di-benzyloxy)-N,N-diethylbenzamide(859103-01-8)
• EPA Substance Registry System: (3,5-di-benzyloxy)-N,N-diethylbenzamide(859103-01-8)

Safety Data

• Hazardous Substances Data: 859103-01-8(Hazardous Substances Data)

Upstream product

• 99-10-5 3,5-Dihydroxybenzoic acid 
• 50513-72-9 (3,5-di-benzyloxy)benzoic acid benzyl ester 
• 109-89-7 diethylamine 
• 100-39-0 benzyl bromide 
• 28917-43-3 3,5-dibenzyloxybenzoic acid 

Downstream Products

• 1017572-30-3 3,5-bis(benzyloxy)-N,N-diethyl-2-formylbenzamide 
• 1017572-28-9 3,5-bis(benzyloxy)-2-bromo-N,N-diethylbenzamide 
• 859103-05-2 phosphoric acid (3-diethylcarbamoyl-5-benzyloxy-phenyl) ester dimethyl ester 
• 859103-50-7 (3-benzyloxy-5-hydroxy)-N,N-diethylbenzamide 

Relevant articles and documents

Synthesis of the Common Monomeric Unit of Uroleuconaphins and Viridaphins via Hauser-Kraus Annulation

A stereoselective synthesis of a pyranonaphthoquinone derivative found in aromatic polyketide-derived aphid pigments is reported herein. This approach features the anionic [4+2]-annulation of phthalides with a carbohydrate-derived optically active enone.