270065-87-7

Basic information

• Product Name: FMOC-(S)-3-AMINO-4-(3-CYANO-PHENYL)-BUTYRIC ACID
• Synonyms: FMOC-3-CYANO-L-BETA-HOMOPHENYLALANINE;FMOC-BETA-HOPHE(3-CN)-OH;FMOC-(S)-3-AMINO-4-(3-CYANOPHENYL)BUTANOIC ACID;FMOC-(S)-3-AMINO-4-(3-CYANO-PHENYL)-BUTYRIC ACID;FMOC-PHE(3-CN)-(C*CH2)OH;N-BETA-(9-FLUORENYLMETHOXYCARBONYL)-L-HOMO(3-CYANOPHENYL)ALANINE;N-(9-FLUORENYLMETHOXYCARBONYL)-(S)-3-AMINO-4-(3-CYANOPHENYL)BUTANOIC ACID;(S)-3-(FMOC-AMINO)-4-(3-CYANOPHENYL)BUTYRIC ACID
• CAS NO: 270065-87-7
• Molecular Formula: C26H22N2O4
• Molecular Weight: 426.46
• Product Categories: 3-Amino-4-phenylbutanoic Acid Analogs;B-Amino
• Mol File: 270065-87-7.mol
• Article Data: 0

Chemical Properties

• Boiling Point: 682.6 °C at 760 mmHg
• Flash Point: 366.6 °C
• Appearance: /
• Density: 1.33 g/cm³
• Vapor Pressure: 1.45E-19mmHg at 25°C
• Refractive Index: 1.662
• Storage Temp.: 2-8°C
• PKA: 4.33±0.10(Predicted)
• CAS DataBase Reference: FMOC-(S)-3-AMINO-4-(3-CYANO-PHENYL)-BUTYRIC ACID(CAS DataBase Reference)
• NIST Chemistry Reference: FMOC-(S)-3-AMINO-4-(3-CYANO-PHENYL)-BUTYRIC ACID(270065-87-7)
• EPA Substance Registry System: FMOC-(S)-3-AMINO-4-(3-CYANO-PHENYL)-BUTYRIC ACID(270065-87-7)

Safety Data

• Safety Statements: 22-24/25
• WGK Germany: 3
• F: 10
• HazardClass: IRRITANT
• Hazardous Substances Data: 270065-87-7(Hazardous Substances Data)

Usage

General Description

FMOC-(S)-3-AMINO-4-(3-CYANO-PHENYL)-BUTYRIC ACID is a chemical compound with potential therapeutic use in the pharmaceutical industry. It is an FMOC-protected amino acid derivative containing both an amino and a carboxylic acid functional group. The (S)-stereochemistry indicates that it is the enantiomer of the compound with the (S) configuration. The presence of the 3-cyano-phenyl group in the molecule makes it a potentially important compound for drug development, as phenyl groups are common in many pharmaceuticals and bioactive compounds. FMOC-(S)-3-AMINO-4-(3-CYANO-PHENYL)-BUTYRIC ACID's structure and properties make it a potentially valuable building block in the synthesis of pharmaceuticals and bioactive compounds, and its (S)-stereochemistry also makes it valuable in the study of stereochemical effects in biological systems.

InChI:InChI=1/C26H22N2O4/c27-15-18-7-5-6-17(12-18)13-19(14-25(29)30)28-26(31)32-16-24-22-10-3-1-8-20(22)21-9-2-4-11-23(21)24/h1-12,19,24H,13-14,16H2,(H,28,31)(H,29,30)/t19-/m0/s1