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2-Fluoro-5-methyl-4-(trifluoromethyl)-DL-phenylalanine

CAS 1435806-24-8Formula C11H11F4NO2MW 265.2PubChem 66523503

This is a phenylalanine derivative featuring a fluorinated and trifluoromethylated phenyl group. It is intended for research applications, particularly in medicinal chemistry or biochemical studies where amino acid analogs with specific steric and electronic properties are required.

Loading RDKit molecule structure...
InChIKey: ZAEBGVLZTPXBJV-UHFFFAOYSA-NC11H11F4NO2 | MW 265.2

Chemical Identity

Molecular Formula

C11H11F4NO2

Molecular Weight

265.2 g/mol

Exact Mass

265.072591

PubChem CID

66523503

IUPAC Name

2-amino-3-[2-fluoro-5-methyl-4-(trifluoromethyl)phenyl]propanoic acid

SMILES String

Cc1cc(CC(N)C(=O)O)c(F)cc1C(F)(F)F

Names & Synonyms

2-Amino-3-(2-fluoro-5-methyl-4-(trifluoromethyl)phenyl)propanoic acid2-Fluoro-5-methyl-4-trifluoromethyl-DL-phenylalanine2-Amino-3-(2-fluoro-5-methyl-4-(trifluoromethyl)phenyl)propanoicacid
External Identifiers
MFCD19687203AKOS015957074

Catalog Overview

2-Fluoro-5-methyl-4-(trifluoromethyl)-DL-phenylalanine (CAS 1435806-24-8) is a synthetic amino acid derivative. Its structure incorporates a phenylalanine backbone substituted with a 2-fluoro, 5-methyl, and 4-trifluoromethyl group on the phenyl ring. This unique substitution pattern introduces specific electronic and steric properties, making it a valuable building block or probe in drug discovery and chemical biology research. As a DL-phenylalanine derivative, it represents a racemic mixture of both D- and L-enantiomers.

Use Context

  • Research chemical sourcing
  • Custom synthesis and catalog availability review
  • COA, SDS, pricing, and fulfillment workflow
Read more catalog context

2-Fluoro-5-methyl-4-(trifluoromethyl)-DL-phenylalanine (CAS 1435806-24-8) is a synthetic amino acid derivative. Its structure incorporates a phenylalanine backbone substituted with a 2-fluoro, 5-methyl, and 4-trifluoromethyl group on the phenyl ring. This unique substitution pattern introduces specific electronic and steric properties, making it a valuable building block or probe in drug discovery and chemical biology research. As a DL-phenylalanine derivative, it represents a racemic mixture of both D- and L-enantiomers. It is primarily used as a research chemical for the synthesis of more complex molecules, investigation of enzyme mechanisms, or as a component in peptidomimetic studies.

Physical Data

Estimated

Estimated / predicted physical property values for catalog reference.

Appearance

White to off-white crystalline powder

Physical State

Solid

Melting Point

200.0 °C

Boiling Point

350.0 °C

Density

1.4 g/cm³

Water Solubility

Sparingly soluble

Flash Point

220.0 °C

Applications / Classifications

Research intermediateCustom synthesis building block

Biological Target Reference

No verified biological target assignment. This compound is listed primarily as a research or synthetic intermediate.

Preliminary Safety-Style Reference

Preliminary

Preliminary safety-style information for reference only. Not a supplier SDS.

Handling and Storage
  • Handle with appropriate personal protective equipment, including gloves, eye protection, and a lab coat. Use in a well-ventilated area or fume hood to avoid inhalation. Avoid contact with skin and eyes. In case of contact, rinse thoroughly with water. Refer to the Safety Data Sheet (SDS) for comprehensive safety information and emergency procedures. Store in a cool, dry place, away from incompatible materials.

Related Products / Graph Discovery

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