288101-16-6

Basic information

• Product Name: (E)-2-(Benzhydrylidene-amino)-5-(2,4-difluoro-phenyl)-5-(4-isopropyl-phenyl)-pent-4-enoic acid methyl ester
• Synonyms: (E)-2-(Benzhydrylidene-amino)-5-(2,4-difluoro-phenyl)-5-(4-isopropyl-phenyl)-pent-4-enoic acid methyl ester
• CAS NO: 288101-16-6
• Molecular Weight: 523.622
• Mol File: 288101-16-6.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: (E)-2-(Benzhydrylidene-amino)-5-(2,4-difluoro-phenyl)-5-(4-isopropyl-phenyl)-pent-4-enoic acid methyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: (E)-2-(Benzhydrylidene-amino)-5-(2,4-difluoro-phenyl)-5-(4-isopropyl-phenyl)-pent-4-enoic acid methyl ester(288101-16-6)
• EPA Substance Registry System: (E)-2-(Benzhydrylidene-amino)-5-(2,4-difluoro-phenyl)-5-(4-isopropyl-phenyl)-pent-4-enoic acid methyl ester(288101-16-6)

Safety Data

• Hazardous Substances Data: 288101-16-6(Hazardous Substances Data)

Upstream product

• 349636-23-3 2-(benzhydrylidene-amino)-5-(4-isopropyl-phenyl)-pent-4-ynoic acid methyl ester 
• 288101-02-0 (Z)-3-(2,4-Difluoro-phenyl)-3-iodo-prop-2-en-1-ol 
• 288101-06-4 1-((Z)-3-Bromo-1-iodo-propenyl)-2,4-difluoro-benzene 
• 288100-99-2 3-(2,4-difluorophenyl)-2-propyn-1-ol 
• 349636-22-2 1-(3-bromo-prop-1-ynyl)-4-isopropyl-benzene 
• 288101-00-8 3-(4-isopropyl-phenyl)-prop-2-yn-1-ol 
• 81167-39-7 methyl N-(diphenylmethylene)glycinate 
• 144025-03-6 2,4-difluorophenylboronic acid 
• 349636-25-5 (E)-2-(Benzhydrylidene-amino)-5-iodo-5-(4-isopropyl-phenyl)-pent-4-enoic acid methyl ester 
• 16152-51-5 (4-isopropylphenyl)boronic acid 
• 288101-10-0 (Z)-2-(Benzhydrylidene-amino)-5-(2,4-difluoro-phenyl)-5-iodo-pent-4-enoic acid methyl ester 
• 2265-93-2 2,4-difluoro-1-iodobenzene 

Downstream Products

• 288101-32-6 (E)-2-Amino-5-(2,4-difluoro-phenyl)-5-(4-isopropyl-phenyl)-pent-4-enoic acid methyl ester 

Relevant articles and documents

Synthesis of chiral and geometrically defined 5,5-diaryl-2-amino-4-pentenoates: Novel amino acid derivatives

A novel series of 5,5-diaryl-2-amino-4-pentenoates were synthesized. Chirally defined substrates were obtained efficiently using Oppolzer's sultam as a chiral auxiliary and a palladium-catalyzed stereoselective hydrostannylation.