70422-07-0

Basic information

• Product Name: N^α-benzoyl-N^ε-(benzyloxycarbonyl)lysine
• CAS NO: 70422-07-0
• Molecular Weight: 384.432
• Mol File: 70422-07-0.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: N^α-benzoyl-N^ε-(benzyloxycarbonyl)lysine(CAS DataBase Reference)
• NIST Chemistry Reference: N^α-benzoyl-N^ε-(benzyloxycarbonyl)lysine(70422-07-0)
• EPA Substance Registry System: N^α-benzoyl-N^ε-(benzyloxycarbonyl)lysine(70422-07-0)

Safety Data

• Hazardous Substances Data: 70422-07-0(Hazardous Substances Data)

Upstream product

• 32302-83-3 N-ε-benzyloxycarbonyl lysine 
• 98-88-4 benzoyl chloride 

Downstream Products

• 123004-03-5 N-<5-Amino-1-(trifluoroacetyl)pentyl>benzamide Hydrochloride 
• 106942-42-1 {4-[5-Oxo-2-phenyl-4-(2,2,2-trifluoro-acetyl)-4,5-dihydro-oxazol-4-yl]-butyl}-carbamic acid benzyl ester 
• 106746-02-5 Phenylmethyl N-<5-(Benzoylamino)-5-(trifluoroacetyl)pentyl>carbamate 
• 123003-97-4 Phenylmethyl N-<4-(4,5-dihydro-5-oxo-2-phenyl-4-oxazoyl)butyl>carbamate 
• 115292-69-8 N²-benzoyl-N⁶-benzyloxycarbonyl-DL-lysine benzyl ester 
• 116783-33-6 N^α-Benzoyllysine 

Relevant articles and documents

SYNTHESIS OF FLUORINATED α-AMINO KETONES PART I: α-BENZAMIDOALKYL MONO- DI- AND TRIFLUOROMETHYL KETONES

2-Phenyl-5(4H)-oxazolones, obtained from α-amino acids, are reacted with di- and trifluoro acetic anhydride by a modified Dakin-West procedure to yield in a one-pot reaction α-benzamidoalkyl-di- and trifluoromethyl ketones in good yields.The monofluoromethyl analogues were also prepared from α-amino acids, however the use of the highly toxic fluoroacetic anhydride was avoided.The key step is the halogen exchange reaction on the corresponding bromomethyl ketone.