142952-86-1

Basic information

• Product Name: L-2-<(benzyloxycarbonyl)amino>-4-(17β-acetyloxyandrost-2-en-3-yl)but-3-enoic acid
• Synonyms: L-2-<(benzyloxycarbonyl)amino>-4-(17β-acetyloxyandrost-2-en-3-yl)but-3-enoic acid
• CAS NO: 142952-86-1
• Molecular Weight: 549.708
• Mol File: 142952-86-1.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: L-2-<(benzyloxycarbonyl)amino>-4-(17β-acetyloxyandrost-2-en-3-yl)but-3-enoic acid(CAS DataBase Reference)
• NIST Chemistry Reference: L-2-<(benzyloxycarbonyl)amino>-4-(17β-acetyloxyandrost-2-en-3-yl)but-3-enoic acid(142952-86-1)
• EPA Substance Registry System: L-2-<(benzyloxycarbonyl)amino>-4-(17β-acetyloxyandrost-2-en-3-yl)but-3-enoic acid(142952-86-1)

Safety Data

• Hazardous Substances Data: 142952-86-1(Hazardous Substances Data)

Upstream product

• 75266-42-1 (S)-2-<(benzyloxycarbonyl)amino>-3-butenoic acid 
• 81827-58-9 17β-acetyloxyandrost-2-en-3-yl trifluoromethanesulphonate 
• 1164-91-6 stanolone acetate 
• 142953-01-3 allyl N-benzyloxycarbonyl-L-vinylglycinate 
• 75266-40-9 N-benzyloxycarbonyl-L-α-vinylglycine methyl ester 

Relevant articles and documents

Palladium-catalyzed heck couplings of L-vinylglycine derivatives with vinyl and aryl halides and triflates

The coupling of aryl and vinyl halides and triflates with L-vinylglycine derivatives under the influence of a palladium catalyst is described. The coupling is regioselective and stereoselective with the absolute configuration of the α-amino acid centre be