57471-70-2

Basic information

• Product Name: diethyl N-benzyloxycarbonyl-(S)-aspartate
• Synonyms: diethyl N-benzyloxycarbonyl-(S)-aspartate
• CAS NO: 57471-70-2
• Molecular Weight: 323.346
• Mol File: 57471-70-2.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: diethyl N-benzyloxycarbonyl-(S)-aspartate(CAS DataBase Reference)
• NIST Chemistry Reference: diethyl N-benzyloxycarbonyl-(S)-aspartate(57471-70-2)
• EPA Substance Registry System: diethyl N-benzyloxycarbonyl-(S)-aspartate(57471-70-2)

Safety Data

• Hazardous Substances Data: 57471-70-2(Hazardous Substances Data)

Upstream product

• 16115-68-7 diethyl L-aspartate hydrochloride 
• 501-53-1 benzyl chloroformate 
• 64-17-5 ethanol 
• 39256-89-8 N-Benzyloxycarbonyl-L-asparaginsaeure-β-aethylester 
• 13552-87-9 L-aspartic acid diethyl ester 

Downstream Products

• 116097-79-1 Z-Asp(OC₂H₅)-Phe-NH₂ 
• 116097-78-0 Z-Asp(OC₂H₅)-Phe-NH-NH-Ph 
• 118219-23-1 [(1S)-3-hydroxy-1-(hydroxymethyl)propyl]carbamic acid phenylmethyl ester 
• 607376-66-9 2-[(4S)-(3-benzyloxycarbonyl-2,2-dimethyl-1,3-oxazolidin-4-y)]ethanol 
• 1602828-00-1 C₃₅H₄₅N₃O₈S₂ 
• 1602827-71-3 C₃₅H₄₅N₃O₈S₂ 
• 1602827-74-6 C₂₆H₃₂N₂O₇S 
• 1602827-77-9 C₂₈H₃₄N₂O₉S 
• 1602827-58-6 C₂₂H₃₀N₂O₇ 
• 607376-67-0 (S)-2,2-dimethyl-4-(2-oxo-ethyl)-oxazolidine-3-carboxylic acid benzyl ester 
• 13552-87-9 L-aspartic acid diethyl ester 
• 87219-29-2 benzyl (3S)-5-oxotetrahydro-3-furanylcarbamate 
• 35677-89-5 benzyl (3S)-2-oxotetrahydro-3-furanylcarbamate 
• 17046-24-1 N-carbonyl-L-aspartic acid diethyl ester 

Relevant articles and documents

Novel pyridinium-type fullerene derivatives as multitargeting inhibitors of HIV-1 reverse transcriptase, HIV-1 protease, and HCV NS5B polymerase

In the present study, we newly synthesized four types of novel fullerene derivatives: pyridinium/ethyl ester-type derivatives 3b?3l, pyridinium/carboxylic acid-type derivatives 4a, 4e, 4f, pyridinium/amide-type derivative 5a, and pyridinium/2-morpholinone

Studies towards the total synthesis of batzelladine A

Application of a diastereoselective three-component coupling to the bicyclic core of the batzelladine alkaloids is described. The synthesis features the elaboration of glutamic acid by use of Eschenmoser sulfide contraction. An earlier approach is also included, which shows some limitations of dithiane chemistry when applied to the particular compounds required for this target.