206268-34-0

Basic information

• Product Name: 1-N-tert-butyloxycarbonyl-4-N-methyl-4-N-(α-N-tosylphenylalanyl)-(1,4)-diaminobutan-2-ol
• Synonyms: 1-N-tert-butyloxycarbonyl-4-N-methyl-4-N-(α-N-tosylphenylalanyl)-(1,4)-diaminobutan-2-ol
• CAS NO: 206268-34-0
• Molecular Weight: 519.662
• Mol File: 206268-34-0.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 1-N-tert-butyloxycarbonyl-4-N-methyl-4-N-(α-N-tosylphenylalanyl)-(1,4)-diaminobutan-2-ol(CAS DataBase Reference)
• NIST Chemistry Reference: 1-N-tert-butyloxycarbonyl-4-N-methyl-4-N-(α-N-tosylphenylalanyl)-(1,4)-diaminobutan-2-ol(206268-34-0)
• EPA Substance Registry System: 1-N-tert-butyloxycarbonyl-4-N-methyl-4-N-(α-N-tosylphenylalanyl)-(1,4)-diaminobutan-2-ol(206268-34-0)

Safety Data

• Hazardous Substances Data: 206268-34-0(Hazardous Substances Data)

Upstream product

• 24424-99-5 di-tert-butyl dicarbonate 
• 206268-15-7 2-methyl-5-tert-butyloxycarbonylaminomethyl-(1,2)-isoxazolidine 
• 78888-18-3 N-tert-butoxycarbonylprop-2-en-1-amine 
• 13505-32-3 N-tosyl-(S)-phenylalanine 
• 206268-20-4 1-N-tert-butyloxycarbonyl-4-N-methyl-(1,4)-diaminobutan-2-ol 
• 34635-34-2 N-tosylphenylalanine 

Relevant articles and documents

Synthesis of perhydrodiazepinones as new putative peptidomimetics

New functionalized 7-membered azaheterocycles (perhydrodiazepinones) have been designed as new scaffolds supposed to mimick peptide γ-turns constrained by an ethylene bridge. They were synthesized by either lactam cyclisation on an aminoacid compound outcoming from a glutamic acid derivative starting material or through an intramolecular Mitsunobu reaction on diaminoalcohol linear precursors. Furthermore, as a new strategy useful for combinatorial chemistry, the second synthesis has been investigated on a soluble polymer support (PEG).