17079-25-3

Basic information

• Product Name: Pentanoic acid, 5-(benzoylamino)-, methyl ester
• CAS NO: 17079-25-3
• Molecular Formula: C13H17NO3
• Molecular Weight: 235.283
• Mol File: 17079-25-3.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Pentanoic acid, 5-(benzoylamino)-, methyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Pentanoic acid, 5-(benzoylamino)-, methyl ester(17079-25-3)
• EPA Substance Registry System: Pentanoic acid, 5-(benzoylamino)-, methyl ester(17079-25-3)

Safety Data

• Hazardous Substances Data: 17079-25-3(Hazardous Substances Data)

Upstream product

• 186581-53-3 diazomethane 
• 15647-47-9 5-benzoylaminopentanoic acid 
• 660-88-8 5-aminopentanoic acid 
• 675-20-7 piperidin-2-one 
• 70-25-7 N-Methyl-N'-nitro-N-nitrosoguanidine 
• 15257-86-0 N-(2-iodo-ethyl)-benzamide 
• 292638-85-8 acrylic acid methyl ester 

Relevant articles and documents

Synthetic studies towards N-substituted 3-vinyl-4-piperidineacetic acid derivatives

The synthesis and full characterization of two new (E)-2-butenyl)-5-amino-2-pentenoates, (Z)-4-[N-(3-buten-1-yl)benzamido]-2-buten-1-ol, and (Z)-1-chloro-4-[N-(3-buten-l-yl)benzamido]-2-butene are reported. These were designed as substrates for a projected thermal ene cyclization leading to the N-substituted 3-vinyl-4-piperidineacetic acid scaffold. Although conditions for this ene-cyclization have not yet been uncovered, the ease of preparation of these ene-cyclization substrates gives promise for their future use.

Identification of the acyclic intermediate in nicotinic acid biosynthesis. 3. Synthesis of beta-carboxy-lysine diastereomers

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