344407-17-6

Basic information

• Product Name: Butanoic acid, 3-[(methoxycarbonyl)amino]-2-methyl-, methyl ester
• Synonyms: Butanoic acid, 3-[(methoxycarbonyl)amino]-2-methyl-, methyl ester
• CAS NO: 344407-17-6
• Molecular Formula: C8H15NO4
• Molecular Weight: 0
• Mol File: 344407-17-6.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• CAS DataBase Reference: Butanoic acid, 3-[(methoxycarbonyl)amino]-2-methyl-, methyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Butanoic acid, 3-[(methoxycarbonyl)amino]-2-methyl-, methyl ester(344407-17-6)
• EPA Substance Registry System: Butanoic acid, 3-[(methoxycarbonyl)amino]-2-methyl-, methyl ester(344407-17-6)

Safety Data

• Hazardous Substances Data: 344407-17-6(Hazardous Substances Data)

Upstream product

• 13592-48-8 (1-methoxy-ethyl)-carbamic acid methyl ester 
• 72658-09-4 (E)-(1-methoxyprop-1-enyloxy)trimethylsilane 
• 67-56-1 methanol 
• 33425-47-7 3,4-dimethylpyrrolidine-2,5-dione 

Relevant articles and documents

Effect of catalytic alkali metal bromide on Hofmann-type rearrangement of imides

The Hofmann-type rearrangement of aromatic and aliphatic imides using KBr as the catalyst proceeded to provide aromatic and aliphatic amino acid derivatives. We have also developed a new synthetic route to gabapentin with this method.

Electroorganic Chemistry. 82. β-Amino Acid Esters from α-Methoxycarbamates and Ketene Silyl Acetals; Cyclization to β-Lactams

A new synthetic method of β-lactams 1'is described.The key intermediates, N-carbomethoxy-β-amino acid esters 2', were synthesized by the reaction of α-methoxylated carbamates 3' with ketene methyl trimethylsilyl acetals 4' catalyzed by titanium tetrachlor