288588-25-0

Basic information

• Product Name: 2-benzyloxycarbonylamino-3-tert-butyldisulfanyl-propionic acid allyl ester
• Synonyms: 2-benzyloxycarbonylamino-3-tert-butyldisulfanyl-propionic acid allyl ester
• CAS NO: 288588-25-0
• Molecular Weight: 383.533
• Mol File: 288588-25-0.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 2-benzyloxycarbonylamino-3-tert-butyldisulfanyl-propionic acid allyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: 2-benzyloxycarbonylamino-3-tert-butyldisulfanyl-propionic acid allyl ester(288588-25-0)
• EPA Substance Registry System: 2-benzyloxycarbonylamino-3-tert-butyldisulfanyl-propionic acid allyl ester(288588-25-0)

Safety Data

• Hazardous Substances Data: 288588-25-0(Hazardous Substances Data)

Upstream product

• 501-53-1 benzyl chloroformate 
• 30044-51-0 S-tert-butylmercapto-L-cysteine 
• 76969-40-9 (R)-2-Benzyloxycarbonylamino-3-tert-butyldisulfanyl-propionic acid 
• 107-18-6 allyl alcohol 

Downstream Products

• 288588-26-1 (R)-2-Benzyloxycarbonylamino-3-phenylsulfanyl-propionic acid allyl ester 
• 82611-65-2 N-benzyloxycarbonyl-S-phenyl-L-cysteine 
• 149034-35-5 Z-Cys-OAll 

Relevant articles and documents

Copper-mediated cross-coupling of aryl boronic acids and alkyl thiols

matrix presented The cross-coupling of aryl boronic acids and alkanethiols mediated by copper(II) acetate and pyridine in anhydrous dimethylformamide affords aryl alkyl sulfides in good yield with a wide variety of substituted aryl boronic acids. The method is applicable to the synthesis of aryl sulfides of cysteine.