1190367-08-8

Basic information

• Product Name: 6-allyl-5-allyloxy-4-(allyl-phenyl-amino)-4'-chloro-3-methyl-biphenyl-2-carboxylic acid ethyl ester
• Synonyms: 6-allyl-5-allyloxy-4-(allyl-phenyl-amino)-4'-chloro-3-methyl-biphenyl-2-carboxylic acid ethyl ester
• CAS NO: 1190367-08-8
• Molecular Weight: 502.053
• Mol File: 1190367-08-8.mol

Chemical Properties

• CAS DataBase Reference: 6-allyl-5-allyloxy-4-(allyl-phenyl-amino)-4'-chloro-3-methyl-biphenyl-2-carboxylic acid ethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: 6-allyl-5-allyloxy-4-(allyl-phenyl-amino)-4'-chloro-3-methyl-biphenyl-2-carboxylic acid ethyl ester(1190367-08-8)
• EPA Substance Registry System: 6-allyl-5-allyloxy-4-(allyl-phenyl-amino)-4'-chloro-3-methyl-biphenyl-2-carboxylic acid ethyl ester(1190367-08-8)

Safety Data

• Hazardous Substances Data: 1190367-08-8(Hazardous Substances Data)

Upstream product

• 106-95-6 allyl bromide 

Downstream Products

• 1190367-25-9 9-(allyl-phenyl-amino)-6-(4-chloro-phenyl)-8-methyl-2,5-dihydro-benzo[b]oxepine-7-carboxylic acid ethyl ester 
• 1190367-24-8 10-allyl-9-(4-chloro-phenyl)-7-methyl-6-phenyl-5,6-dihydro-2H-benzo[b][1,4]oxazocine-8-carboxylic acid ethyl ester 

Relevant articles and documents

High-yielding synthesis of Nefopam analogues (functionalized benzoxazocines) by sequential one-pot cascade operations

An efficient amine-/ruthenium-catalyzed three-step process for the synthesis of Nefopam analogues was achieved through combinations of cascade enamine amination/iso-aromatization/allylation and diene or enyne metathesis as key steps starting from functionalized Hagemann's esters. In this communication, we discovered the application of ruthenium-catalysis on olefins containing free amines without in situ formation of salts.