1207459-96-8

Basic information

• Product Name: ethyl (2E,5S)-5-(4-methoxyphenylamino)-5-(pyridin-3-yl)pent-2-enoate
• Synonyms: ethyl (2E,5S)-5-(4-methoxyphenylamino)-5-(pyridin-3-yl)pent-2-enoate
• CAS NO: 1207459-96-8
• Molecular Weight: 326.395
• Mol File: 1207459-96-8.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: ethyl (2E,5S)-5-(4-methoxyphenylamino)-5-(pyridin-3-yl)pent-2-enoate(CAS DataBase Reference)
• NIST Chemistry Reference: ethyl (2E,5S)-5-(4-methoxyphenylamino)-5-(pyridin-3-yl)pent-2-enoate(1207459-96-8)
• EPA Substance Registry System: ethyl (2E,5S)-5-(4-methoxyphenylamino)-5-(pyridin-3-yl)pent-2-enoate(1207459-96-8)

Safety Data

• Hazardous Substances Data: 1207459-96-8(Hazardous Substances Data)

Upstream product

• 41855-73-6 3-<(4-methoxyphenyl)iminomethyl>pyridine 
• 96995-10-7 tert-butyl((1-ethoxybuta-1,3-dien-1-yl)oxy)dimethylsilane 

Downstream Products

• 1207459-97-9 ethyl (5S)-5-(4-methoxyphenylamino)-5-(pyridin-3-yl)pentanoate 

Relevant articles and documents

A straightforward synthesis of (S)-Anabasine via the catalytic, enantioselective vinylogous mukaiyama-Mannich reaction

The tobacco alkaloid (S)-anabasine was synthesized by a straightforward 4-step sequence with the catalytic enantioselective vinylogous Mannich reaction as a key step. Only 3 mol% of a structurally optimized chiral BINOL-based phosphoric acid was employed to control the absolute configuration of the natural product. Georg Thieme Verlag Stuttgart.