117710-12-0

Basic information

• Product Name: L-Threonine, N-[(phenylmethoxy)carbonyl]-, 2-propenyl ester
• CAS NO: 117710-12-0
• Molecular Formula: C15H19NO5
• Molecular Weight: 293.32
• Mol File: 117710-12-0.mol

Chemical Properties

• CAS DataBase Reference: L-Threonine, N-[(phenylmethoxy)carbonyl]-, 2-propenyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: L-Threonine, N-[(phenylmethoxy)carbonyl]-, 2-propenyl ester(117710-12-0)
• EPA Substance Registry System: L-Threonine, N-[(phenylmethoxy)carbonyl]-, 2-propenyl ester(117710-12-0)

Safety Data

• Hazardous Substances Data: 117710-12-0(Hazardous Substances Data)

Upstream product

• 19728-63-3 N-[(phenylmethoxy)carbonyl]-L-threonine 
• 106-95-6 allyl bromide 
• 88224-11-7 L-threonine allyl ester p-toluene sulfonate 
• 501-53-1 benzyl chloroformate 
• 19728-63-3 N-benzyloxycarbonyl-L-treonine 
• 107-18-6 allyl alcohol 

Downstream Products

• 118398-57-5 N-(benzyloxycarbonyl)-O-(3,4,6-tri-O-acetyl-2-acetamido-2-deoxy-α-D-galactopyranosyl)threonyl-N⁴-(3,4,6-tri-O-acetyl-2-acetamido-2-deoxy-β-D-glucopyranosyl)asparagine allyl ester 
• 118417-77-9 C₃₅H₄₅N₂O₁₂P 
• 118417-78-0 N-(benzyloxycarbonyl)-O-(3,4,6-tri-O-acetyl-2-acetamido-2-deoxy-α-D-galactopyranosyl)threonine allyl ester 
• 118417-79-1 N-(benzyloxycarbonyl)-O-(2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-α-D-galactopyranosyl)-L-threonine 
• 118490-32-7 N-(benzyloxycarbonyl)-O-(2,3,4-tri-O-acetyl-2-azido-2-deoxy-β-D-galactopyranosyl)threonine allyl ester 
• 118417-76-8 N-(benzyloxycarbonyl)-O-(3,4,6-tri-O-acetyl-2-azido-2-deoxy-α-D-galactopyranosyl)threonine allyl ester 
• 117710-23-3 (S)-2-Benzyloxycarbonylamino-3-[(S)-3-(4-methoxy-phenyl)-2-methylamino-propionyloxy]-butyric acid allyl ester; compound with trifluoro-acetic acid 
• 117710-13-1 allyl N-(benzyloxycarbonyl)-O--L-threoninate 

Relevant articles and documents

Simple and mild esterification of N-protected amino acids with nearly equimolar amounts of alcohols using 1-tert-butoxy-2-tert-butoxycarbonyl-1,2- dihydroisoquinoline

A very mild, one-step esterification using nearly equimolar amounts of N-protected amino acids and alcohols, in conjunction with 1-tert-butoxy-2-tert- butoxycarbonyl-1,2-dihydroisoquinoline (BBDI) as a novel condensing reagent is described.

Allyl Esters as Carboxy Protecting Groups in the Synthesis of O-Glycopeptides

The construction of β-D-xylosyl- and α-D-N-acetylgalactosaminylserine and -threonine glycopeptides is carried out by using the allyl ester for selective C-terminal deprotection.The β-glycosidic bond between N-(benzyloxycarbonyl)serine allyl ester and 2,3,