252940-43-5

Basic information

• Product Name: Boc-NH-CH((CH₂)3NHZ)-CH₂-S-(CH₂)3COOtBu
• CAS NO: 252940-43-5
• Molecular Weight: 510.695
• Mol File: 252940-43-5.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: Boc-NH-CH((CH₂)3NHZ)-CH₂-S-(CH₂)3COOtBu(CAS DataBase Reference)
• NIST Chemistry Reference: Boc-NH-CH((CH₂)3NHZ)-CH₂-S-(CH₂)3COOtBu(252940-43-5)
• EPA Substance Registry System: Boc-NH-CH((CH₂)3NHZ)-CH₂-S-(CH₂)3COOtBu(252940-43-5)

Safety Data

• Hazardous Substances Data: 252940-43-5(Hazardous Substances Data)

Upstream product

• 110661-91-1 tert-butyl 4-bromobutyrate 
• 252940-40-2 (4-tert-butoxycarbonylamino-5-mercapto-pentyl)-carbamic acid benzyl ester 
• 233689-90-2 Boc-NH-CH((CH₂)3NHZ)-CH₂-S-CO-CH₃ 
• 105562-75-2 N²-(tert-butyloxycarbonyl)-N⁵-(benzyloxycarbonyl)-2(S),5-diaminopentanol 

Downstream Products

• 252940-46-8 4-((S)-2-Amino-5-benzyloxycarbonylamino-pentylsulfanyl)-butyric acid 

Relevant articles and documents

The synthesis of a new class of oxytocin antagonists

The synthesis of a new class of oxytocin antagonists, with significantly modified C-terminal part, is described. The chemistry of the Mitsunobu reaction was applied to obtain the key derivatives. In spite of the extensive modifications of previously described compound F792, the peptides retain biological activity as oxytocin antagonists.