β,β-Diphenyl-DL-alanine
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β,β-Diphenyl-DL-alanine

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Category
DL-Amino Acids
Catalog number
BAT-007530
CAS number
62653-26-3
Molecular Formula
C15H15NO2
Molecular Weight
241.29
β,β-Diphenyl-DL-alanine
IUPAC Name
2-amino-3,3-diphenylpropanoic acid
Synonyms
H-DL-Dph-OH; H-DL-(β-Phenyl)Phe-OH; β-Phenyl-DL-phenylalanine; DL-Ala(3,3-Dipheyl)-OH; 3,3-Diphenyl-DL-alanine; 2-Amino-3,3-diphenylpropionic acid; 3,3-DIPHENYL-DL-ALANINE; H-beta,beta-Diphenyl-DL-Ala-OH; (2R)-2-amino-3,3-diphenylpropanoic acid; (S)-2-Amino-3,3-diphenylpropionic acid; H DL Dph OH
Appearance
Pale white solid
Purity
≥ 98% (HPLC)
Density
1.198±0.06 g/cm3 (Predicted)
Melting Point
236 °C (dec.)
Boiling Point
389.2±30.0 °C (Predicted)
Storage
Store at 2-8 °C
InChI
InChI=1S/C15H15NO2/c16-14(15(17)18)13(11-7-3-1-4-8-11)12-9-5-2-6-10-12/h1-10,13-14H,16H2,(H,17,18)
InChI Key
PECGVEGMRUZOML-UHFFFAOYSA-N
Canonical SMILES
C1=CC=C(C=C1)C(C2=CC=CC=C2)C(C(=O)O)N

β,β-Diphenyl-DL-alanine, an amino acid derivative renowned for its distinctive structural characteristics, finds applications across diverse scientific sectors. Here, delve into the key applications of β,β-Diphenyl-DL-alanine, presented with a high degree of perplexity and burstiness:

Pharmaceutical Development: Acting as a foundational element for pharmaceutical compound synthesis, β,β-Diphenyl-DL-alanine contributes its unique structural attributes to boost the stability, bioavailability, and therapeutic effectiveness of drug formulations. Researchers are exploring its potential in crafting medications tailored to combat specific ailments, ranging from neurological disorders to various forms of cancer, pushing the boundaries of targeted therapeutics.

Chemical Synthesis: Within organic chemistry, β,β-Diphenyl-DL-alanine serves as a pivotal intermediate for generating intricate molecules. By offering a chiral center, it facilitates the creation of stereoisomer-specific compounds crucial in pharmaceutical and agrochemical development. The adaptability of this amino acid derivative proves invaluable in producing a myriad of chemical entities, showcasing its versatility in advancing chemical synthesis practices.

Peptide Research: Integrating this compound into peptide chains opens avenues for probing protein structure and function. Through the substitution of natural amino acids with β,β-Diphenyl-DL-alanine, researchers embark on explorations into peptide conformation and stability, elucidating critical insights into protein interactions. These investigations are instrumental in unraveling protein dynamics and paving the way for designing innovative peptides with therapeutic potency, enriching the landscape of peptide research.

Biomaterial Design: Employing β,β-Diphenyl-DL-alanine in the development of novel biomaterials for medical applications unleashes a realm of possibilities. Its integration into polymer matrices elevates the mechanical properties and biocompatibility of materials destined for implants, drug delivery systems, and tissue engineering scaffolds. This enhancement not only boosts the performance and longevity of biomedical devices but also opens new horizons for biomaterial innovation, fueling advancements in medical technology.

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