Research chemical
CAS Number: 1270137-96-6
Product details
For laboratory research and professional procurement workflows.
PubChem CID
92964034
Exact Mass
251.056941
InChIKey
OMTZLRBOGCVOEM-QMMMGPOBSA-N
IUPAC Name
(2S)-2-amino-3-[2-fluoro-4-(trifluoromethyl)phenyl]propanoic acid
SMILES String
N[C@@H](Cc1ccc(C(F)(F)F)cc1F)C(=O)O
Appearance
Catalog navigation
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(S)-2-Amino-3-(2-fluoro-4-(trifluoromethyl)phenyl)propanoic acid is identified by CAS 1270137-96-6, with molecular formula C10H9F4NO2, molecular weight 251.18, InChIKey OMTZLRBOGCVOEM-QMMMGPOBSA-N.
Yes. Submit an RFQ and specify COA requirements. Lot-specific COA depends on supplier confirmation.
Yes. Supplier SDS can be requested through the RFQ workflow before handling, storage, shipment, or procurement decisions.
Availability, pack size, lead time, and pricing are confirmed through RFQ.
Submit the CAS number, quantity, purity requirement, and destination country for sourcing review.
White crystalline powder
Physical State
Solid
Melting Point
180.0 °C
Boiling Point
380.0 °C
Density
1.5 g/cm³
Water Solubility
Slightly soluble to soluble
Flash Point
230.0 °C
Vapor Pressure
Estimated very low; unit not specified
Autoignition Temp
450.0 °C
Properties are provided as catalog reference data and may be confirmed through supplier documentation when required.
Heavy atom count
17
H-bond acceptors
3
H-bond donors
3
Rotatable bonds
3
Ring count
1
Aromatic rings
1
Topological polar surface area
63.32 Ų
Computed LogP
1.8
Fragment-like structure rule
Yes
Lead-like structure rule
Yes
Drug-like structure rule
Yes
Structure family
n heterocycle ligand
Precious metal motif
No
Transition metal motif
No
Phosphine ligand motif
No
N-heterocycle motif
Yes
Boronic acid motif
No
Computed structure descriptors generated from molecular structure. These are not experimental physical property values, supplier specifications, SDS data, or bioactivity claims.
Structural features
(S)-2-Amino-3-(2-fluoro-4-(trifluoromethyl)phenyl)propanoic acid is a fluorinated derivative of the essential amino acid L-phenylalanine.
Sourcing context
Catalog reference for RFQ preparation, supplier confirmation, and research chemical sourcing review.
Research use context
This compound is suitable for research applications in synthetic organic chemistry, medicinal chemistry, and biochemistry, particularly for the synthesis of modified peptides, peptidomimetics, and small molecule drug candidates.
Documentation needs
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.
Safety and handling reference content is available through documentation requests.
For supplier-issued SDS, request documentation before handling, storage, shipment, or procurement decisions.