109579-23-9

Basic information

• Product Name: BOC-(3S,4S)-4-AMINO-3-HYDROXY-5-(3-INDOLYL)-PENTANOIC ACID
• Synonyms: BOC-(3S,4S)-4-AMINO-3-HYDROXY-5-(3-INDOLYL)-PENTANOIC ACID;BOC-AHIPA;BOC-AHIPA-OH;Boc-(3S,4S)-4-amino-3-hydroxy-5-(1H-indol-3-yl)-pentanoic acid;Boc-(3S,4S)-4-amino-3-hydroxy-5-(3-indolyl)pentanoic acid≥ 97% (HPLC);Boc-AHIPA(3S,4S)-OH
• CAS NO: 109579-23-9
• Molecular Formula: C18H24N2O5
• Molecular Weight: 348.39
• Mol File: 109579-23-9.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 631.1±55.0 °C(Predicted)
• Appearance: /
• Density: 1.280±0.06 g/cm3(Predicted)
• Storage Temp.: Store at 0-5°C
• PKA: 4.24±0.10(Predicted)
• CAS DataBase Reference: BOC-(3S,4S)-4-AMINO-3-HYDROXY-5-(3-INDOLYL)-PENTANOIC ACID(CAS DataBase Reference)
• NIST Chemistry Reference: BOC-(3S,4S)-4-AMINO-3-HYDROXY-5-(3-INDOLYL)-PENTANOIC ACID(109579-23-9)
• EPA Substance Registry System: BOC-(3S,4S)-4-AMINO-3-HYDROXY-5-(3-INDOLYL)-PENTANOIC ACID(109579-23-9)

Safety Data

• Hazardous Substances Data: 109579-23-9(Hazardous Substances Data)

Usage

Chemical Properties

White powder

Upstream product

• 112700-46-6 (5S)-4-hydroxy-5-indol-3-ylmethyl-1-t-butoxycarbonylaminopyrrol-2(5H)-one 
• 13139-14-5 N-(tert-Butyloxycarbonyl)-L-tryptophan 
• 112700-50-2 (4S,5S)-4-hydroxy-5-indol-3-ylmethyl-1-t-butoxycarbonylaminopyrrol-2-one 

Relevant articles and documents

Stereospecific Synthesis of N-Protected Statine and Its Analogues via Chiral Tetramic Acid

The condensation of a chiral N-protected amino acid with Meldrum's acid in the presence of isopropenyl chloroformate (IPCF) and of 4-N,N-dimethylaminopyridine (DMAP) has been examined.The cyclisation of the reaction product, by heating in an organic solve