24958-43-8

Basic information

• Product Name: 5-benzyloxy-N-[2-(4-benzyloxy-phenyl)-ethyl]-2-bromo-4-methoxy-N-methylbenzamide
• Synonyms: 5-benzyloxy-N-[2-(4-benzyloxy-phenyl)-ethyl]-2-bromo-4-methoxy-N-methylbenzamide
• CAS NO: 24958-43-8
• Molecular Weight: 560.487
• Mol File: 24958-43-8.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: 5-benzyloxy-N-[2-(4-benzyloxy-phenyl)-ethyl]-2-bromo-4-methoxy-N-methylbenzamide(CAS DataBase Reference)
• NIST Chemistry Reference: 5-benzyloxy-N-[2-(4-benzyloxy-phenyl)-ethyl]-2-bromo-4-methoxy-N-methylbenzamide(24958-43-8)
• EPA Substance Registry System: 5-benzyloxy-N-[2-(4-benzyloxy-phenyl)-ethyl]-2-bromo-4-methoxy-N-methylbenzamide(24958-43-8)

Safety Data

• Hazardous Substances Data: 24958-43-8(Hazardous Substances Data)

Upstream product

• 27240-64-8 5-Benzyloxy-2-bromo-4-methoxybenzoylchlorid 
• 24958-41-6 N-methyl-O-benzyltyramine hydochloride 
• 24958-42-7 2-bromo-4-methoxy-5-benzyloxy-benzoic acid 
• 38961-21-6 [2-(4-benzyloxy-phenyl)-ethyl]methylamine 
• 873195-14-3 5-benzyloxy-2-bromo-4-methoxy benzoic acid benzotriazole-1-yl ester 

Downstream Products

• 24958-44-9 2-bromo-4-methoxy-5-hydroxy-N-[2-(4-hydroxyphenyl)-ethyl]-N-methylbenzamide 

Relevant articles and documents

Syntheses and Preparations of Narwedine and Related Novel Compounds

The present invention relates to a process for preparing racemic narwedine (which can be can be kinetically resolved) to yield (?)-narwedine and which is the biogenic precursor of (?)-galanthamine) and the use thereof as a starting material for producing (?)-galanthamine. The invention further includes processes for preparing (?)-galanthamine and (?)-galanthamine hydrobromide, as well as related novel compounds.

PROCESS FOR PREPARATION OF BENZAZEPINE

This invention discloses a process for manufacture of galanthamine, which involves a stereoselective reduction step to get the desired isomer of galanthamine. The current embodiment also discusses the method for improving the chiral and chemical purity of galanthamine and galanthamine salts.

Processes for the preparation of derivatives of 4a, 5, 9, 10, 11, 12-hexahydro-6H-benzofuro-[3a, 3, 2-ef][2]benzazepine

The invention relates to processes for the preparation of 4a,5,9,10,11,12-hexahydro-6H-benzofuro[3a,3,2-ef][2]benzazepine, or derivatives thereof. Furthermore, the invention also relates to the compounds formed during the preparation of 4a, 5,9,10,11,12-hexahydro-6H-benzofuro[3a,3,2-ef][2]benzazepine.