1425667-40-8

Basic information

• Product Name: (R,E)-ethyl [8-(4-nitrophenyl)-6-oxo-oct-7-en-4-yl]carbamate
• Synonyms: (R,E)-ethyl [8-(4-nitrophenyl)-6-oxo-oct-7-en-4-yl]carbamate
• CAS NO: 1425667-40-8
• Molecular Weight: 334.372
• Mol File: 1425667-40-8.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: (R,E)-ethyl [8-(4-nitrophenyl)-6-oxo-oct-7-en-4-yl]carbamate(CAS DataBase Reference)
• NIST Chemistry Reference: (R,E)-ethyl [8-(4-nitrophenyl)-6-oxo-oct-7-en-4-yl]carbamate(1425667-40-8)
• EPA Substance Registry System: (R,E)-ethyl [8-(4-nitrophenyl)-6-oxo-oct-7-en-4-yl]carbamate(1425667-40-8)

Safety Data

• Hazardous Substances Data: 1425667-40-8(Hazardous Substances Data)

Upstream product

• 2396-77-2 methyl 2-hexenoate 
• 1425666-76-7 C₁₀H₁₉NO₄ 
• 1425666-91-6 (R)-ethyl [1-(diethoxyphosphoryl)-2-oxoheptan-4-yl]carbamate 
• 555-16-8 4-nitrobenzaldehdye 
• 208447-08-9 (R)-3-Amino-hexanoic acid methyl ester 

Relevant articles and documents

Efficient synthesis of β'-amino-α, β-unsaturated ketones

A general and simple procedure to access chiral β'-amino-α, β-enones, in seven steps, from an α,β unsaturated ester has been described. The use of a Horner-Wadsworth-Emmons reaction as a key step for generating the β'-amino-α,β-enones, permits access to a range of substrates under mild conditions and in moderate to high yield.