133602-34-3

Basic information

• Product Name: N-(3-Carbethoxypropanoyl)-ω-aminoacetophenone
• Synonyms: N-(3-Carbethoxypropanoyl)-ω-aminoacetophenone
• CAS NO: 133602-34-3
• Molecular Weight: 263.293
• Mol File: 133602-34-3.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: N-(3-Carbethoxypropanoyl)-ω-aminoacetophenone(CAS DataBase Reference)
• NIST Chemistry Reference: N-(3-Carbethoxypropanoyl)-ω-aminoacetophenone(133602-34-3)
• EPA Substance Registry System: N-(3-Carbethoxypropanoyl)-ω-aminoacetophenone(133602-34-3)

Safety Data

• Hazardous Substances Data: 133602-34-3(Hazardous Substances Data)

Upstream product

• 14794-31-1 ethyl 3-(chloroformyl)propionate 
• 5468-37-1 2-aminoacetophenone hydrochloride 

Downstream Products

• 23485-68-9 3-(5'-Phenyl-2'-oxazolyl)propanoic Acid 
• 133602-41-2 N'-Carbethoxy-2-(5'-phenyl-2'-oxazolyl)propanoic Hydrazide 
• 133602-45-6 2,3,5,6-Tetrahydro-5-oxo-2-benzoyl-3-carbethoxy-1,2,4-triazolo<2,3-a>pyrrole 
• 133602-38-7 2-(2-Carbethoxyethyl)-5-phenyloxazole 

Relevant articles and documents

Novel Heterocycles by Bis Heteroannulation of Oxazoles

We report the first examples of intramolecular Diels-Alder addition of heterodienophiles N=N, C=N, C=O, C=S to oxazoles.The required 5-ethoxy- and 5-phenyloxazoles were synthesized bearing a side chain of variable length on C-2 to which the different heterodienophiles are attached.The products of the thermal bis heteroannulation are 3-triazolines, imidazolines, oxazolines, or thiazolines fused to a five- to six-membered ring.Relative reactivities were established and the mechanism is discussed.