579466-93-6

Basic information

• Product Name: Glycine, N-(2-methyl-2-propenyl)-N-[(phenylmethoxy)carbonyl]-, ethyl ester
• CAS NO: 579466-93-6
• Molecular Formula: C16H21NO4
• Molecular Weight: 291.347
• Mol File: 579466-93-6.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: Glycine, N-(2-methyl-2-propenyl)-N-[(phenylmethoxy)carbonyl]-, ethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Glycine, N-(2-methyl-2-propenyl)-N-[(phenylmethoxy)carbonyl]-, ethyl ester(579466-93-6)
• EPA Substance Registry System: Glycine, N-(2-methyl-2-propenyl)-N-[(phenylmethoxy)carbonyl]-, ethyl ester(579466-93-6)

Safety Data

• Hazardous Substances Data: 579466-93-6(Hazardous Substances Data)

Upstream product

• 1458-98-6 2-methyl-3-bromo-1-propene 
• 1145-81-9 ethyl 2-(benzyloxycarbonylamino)ethanoate 

Downstream Products

• 579467-28-0 3-hydroxymethyl-8a-methyl-5-oxo-hexahydro-oxazolo[3,2-a]pyrazine-7-carboxylic acid benzyl ester 
• 579466-96-9 [benzyloxycarbonyl-(2-oxo-propyl)-amino]-acetic acid 
• 579466-95-8 [benzyloxycarbonyl-(2-oxo-propyl)-amino]-acetic acid ethyl ester 

Relevant articles and documents

Efficient, stereoselective synthesis of oxazolo[3,2-a]pyrazin-5-ones: Novel bicyclic lactam scaffolds from the bicyclocondensation of 3-aza-1,5-ketoacids and amino alcohols

(Matrix presented) The bicyclocondensation of 3-aza-1,5-ketoacids and amino alcohols furnished novel oxazolo[3,2-a]pyrazin-5-one scaffolds possessing angular, ring junction substituents in high yield with excellent levels of substrate-based diastereocontr