🌟 99% Happy customers

📦 Same-day shipping on in-stock items

Catalog Number:
16721
CAS Number:
1217733-31-7
Boc-(2R,3R-3-amino-2-hydroxy-3-(4-trifluoromethylphenyl)propionic acid
Purity:
≥ 97% (HPLC)
Documents
$93.14 /25MG
Pack Size Availability Price
Request Bulk Quote
Product Information

Boc-(2R,3R)-3-amino-2-hydroxy-3-(4-trifluoromethylphenyl)propionic acid is a versatile compound widely utilized in pharmaceutical research and development. This amino acid derivative features a unique trifluoromethyl group, enhancing its bioactivity and making it a valuable building block in the synthesis of various biologically active molecules. Its Boc (tert-butyloxycarbonyl) protecting group allows for selective deprotection, facilitating further functionalization in peptide synthesis and medicinal chemistry applications.

Researchers appreciate this compound for its potential in developing novel therapeutics, particularly in the fields of neuropharmacology and oncology. Its structural characteristics enable it to interact effectively with biological targets, paving the way for innovative drug design. The compound's stability and reactivity make it an ideal candidate for incorporation into complex molecular frameworks, thus expanding its utility in synthetic organic chemistry.

CAS Number
1217733-31-7
Purity
≥ 97% (HPLC)
Molecular Formula
C15H18F3NO5
Molecular Weight
349.3
MDL Number
MFCD07363581
PubChem ID
21219553
Melting Point
163-172 °C
Appearance
White powder
Optical Rotation
[a]D25 = -32 ± 2º (C=1 in EtOH)
Conditions
Store at 0-8°C
General Information
CAS Number
1217733-31-7
Purity
≥ 97% (HPLC)
Molecular Formula
C15H18F3NO5
Molecular Weight
349.3
MDL Number
MFCD07363581
PubChem ID
21219553
Melting Point
163-172 °C
Appearance
White powder
Optical Rotation
[a]D25 = -32 ± 2º (C=1 in EtOH)
Conditions
Store at 0-8°C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Boc-(2R,3R)-3-amino-2-hydroxy-3-(4-trifluoromethylphenyl)propionic acid is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a valuable building block in the synthesis of peptides, allowing researchers to create complex structures with specific biological activities.
  • Drug Development: Its unique properties make it a candidate for developing new pharmaceuticals, particularly in targeting specific receptors due to its structural characteristics.
  • Bioconjugation: The compound can be used to attach biomolecules to surfaces or other molecules, enhancing the functionality of diagnostic tools and therapeutic agents.
  • Research in Neuroscience: It is being investigated for its potential effects on neurotransmitter systems, which could lead to advancements in treatments for neurological disorders.
  • Fluorinated Compound Applications: The trifluoromethyl group provides unique electronic properties, making it useful in materials science for developing advanced polymers and coatings.

Citations