216007-00-0

Basic information

• Product Name: (S)-2-Amino-3-(4-isopropyl-phenyl)propionic acid
• Synonyms: 4-(1-Methylethyl)-L-phenylalanine
• CAS NO: 216007-00-0
• Molecular Formula: C12H17NO2
• Molecular Weight: 207.27
• Mol File: 216007-00-0.mol

Chemical Properties

• Melting Point: 255 °C
• Boiling Point: 340.6±30.0 °C(Predicted)
• Appearance: /
• Density: 1.105±0.06 g/cm3(Predicted)
• PKA: 2.23±0.10(Predicted)
• CAS DataBase Reference: (S)-2-Amino-3-(4-isopropyl-phenyl)propionic acid(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-2-Amino-3-(4-isopropyl-phenyl)propionic acid(216007-00-0)
• EPA Substance Registry System: (S)-2-Amino-3-(4-isopropyl-phenyl)propionic acid(216007-00-0)

Safety Data

• Hazardous Substances Data: 216007-00-0(Hazardous Substances Data)

Usage

Uses

Used in Chemical Analysis:
(S)-2-Amino-3-(4-isopropyl-phenyl)propionic acid is used as a reagent for [specific analytical purpose] in chemical analysis, due to its unique structural properties that allow for specific interactions with other compounds.
Used in Organic Synthesis:
(S)-2-Amino-3-(4-isopropyl-phenyl)propionic acid is used as a building block for [specific synthesis process] in organic synthesis, where its distinct structure contributes to the formation of complex molecules.
Used in Pharmaceutical Industry:
(S)-2-Amino-3-(4-isopropyl-phenyl)propionic acid is used as a precursor for [specific drug development] in the pharmaceutical industry, where its unique properties may be leveraged to create novel therapeutic agents.
Used in Research and Development:
(S)-2-Amino-3-(4-isopropyl-phenyl)propionic acid is used as a research compound for [specific scientific investigation] in research and development, where its properties are explored for potential applications in various fields.

Upstream product

• 3368-21-6 (E)-4-isopropylcinnamic acid 
• 849585-22-4 LACTIC ACID 

Relevant articles and documents

Organocatalytic Enantioselective Addition of α-Aminoalkyl Radicals to Isoquinolines

With a dual organocatalytic system involving a chiral phosphoric acid and a dicyanopyrazine-derived chromophore (DPZ) photosensitizer and under the irradiation with visible light, an enantioselective Minisci-type addition of α-amino acid-derived redox-active esters (RAEs) to isoquinolines has been developed. A variety of prochiral α-aminoalkyl radicals generated from RAEs were successfully introduced on isoquinolines, providing a range of valuable α-isoquinoline-substituted chiral secondary amines in high yields with good to excellent enantioselectivities.

Phenylalanine aminomutase-catalyzed addition of ammonia to substituted cinnamic acids: A route to enantiopure α- and β-amino acids

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