270065-80-0

Basic information

• Product Name: BOC-(S)-3-AMINO-4-(4-TRIFLUOROMETHYL-PHENYL)-BUTYRIC ACID
• Synonyms: BOC-BETA-HOPHE(4-CF3)-OH;BOC-4-(TRIFLUOROMETHYL)-L-BETA-HOMOPHENYLALANINE;BOC-(S)-3-AMINO-4-(4-TRIFLUOROMETHYLPHENYL)BUTANOIC ACID;BOC-(S)-3-AMINO-4-(4-TRIFLUOROMETHYL-PHENYL)-BUTYRIC ACID;BOC-PHE(4-CF 3)-(C*CH2)OH;N-T-BUTOXYCARBONYL-(S)-3-AMINO-4-(4-TRIFLUOROMETHYLPHENYL)BUTANOIC ACID;N-BETA-T-BUTOXYCARBONYL-L-HOMO(4-TRIFLUOROMETHYLPHENYL)ALANINE;(S)-BOC-4-(TRIFLUOROMETHYL)-BETA-HOMOPHE-OH
• CAS NO: 270065-80-0
• Molecular Formula: C₁₆H₂₀F₃NO₄
• Molecular Weight: 347.33
• Product Categories: 3-Amino-4-phenylbutanoic Acid Analogs;B-Amino
• Mol File: 270065-80-0.mol
• Article Data: 0

Chemical Properties

• Boiling Point: 449.7 °C at 760 mmHg
• Flash Point: 225.8 °C
• Appearance: /
• Density: 1.246
• Vapor Pressure: 7.1E-09mmHg at 25°C
• Refractive Index: 1.486
• PKA: 4.38±0.10(Predicted)
• CAS DataBase Reference: BOC-(S)-3-AMINO-4-(4-TRIFLUOROMETHYL-PHENYL)-BUTYRIC ACID(CAS DataBase Reference)
• NIST Chemistry Reference: BOC-(S)-3-AMINO-4-(4-TRIFLUOROMETHYL-PHENYL)-BUTYRIC ACID(270065-80-0)
• EPA Substance Registry System: BOC-(S)-3-AMINO-4-(4-TRIFLUOROMETHYL-PHENYL)-BUTYRIC ACID(270065-80-0)

Safety Data

• Safety Statements: 22-24/25
• WGK Germany: 3
• F: 10
• HazardClass: IRRITANT
• Hazardous Substances Data: 270065-80-0(Hazardous Substances Data)

Usage

General Description

The chemical BOC-(S)-3-amino-4-(4-trifluoromethyl-phenyl)-butyric acid is a compound with a molecular formula C14H17F3NO4. It is a derivative of the amino acid butyric acid and features a BOC (tert-butoxycarbonyl) protective group to prevent unwanted reactions. BOC-(S)-3-AMINO-4-(4-TRIFLUOROMETHYL-PHENYL)-BUTYRIC ACID is widely used in the pharmaceutical industry as a building block for the synthesis of various pharmaceutical drugs and biologically active molecules. Its trifluoromethyl group makes it an important building block in medicinal chemistry for the development of drugs with improved pharmacological properties. Additionally, its chiral nature makes it an important component for the synthesis of chiral drugs and pharmaceutical compounds.

InChI:InChI=1/C16H20F3NO4/c1-15(2,3)24-14(23)20-12(9-13(21)22)8-10-4-6-11(7-5-10)16(17,18)19/h4-7,12H,8-9H2,1-3H3,(H,20,23)(H,21,22)/t12-/m0/s1

Downstream Products

• 864775-43-9 1,1-dimethylethyl ((1S)-3-hydroxy-1-{[4-(trifluoromethyl)phenyl]methyl}propyl)carbamate