Z-3-(2-naphthyl)-D-alanine
Need Assistance?
  • US & Canada:
    +
  • UK: +

Z-3-(2-naphthyl)-D-alanine

* Please kindly note that our products are not to be used for therapeutic purposes and cannot be sold to patients.

Category
CBZ-Amino Acids
Catalog number
BAT-005744
CAS number
143218-10-4
Molecular Formula
C21H19NO4
Molecular Weight
349.37
Z-3-(2-naphthyl)-D-alanine
IUPAC Name
(2R)-3-naphthalen-2-yl-2-(phenylmethoxycarbonylamino)propanoic acid
Synonyms
Z-D-Ala(2-naphthyl)-OH; (2R)-2-([(Benzyloxy)carbonyl]amino)-3-naphthalen-2-yl-propionic acid
Appearance
White to off-white powder
Purity
≥ 98% (HPLC)
Density
1.275g/cm3
Melting Point
107-113 °C
Boiling Point
591.4°C at 760 mmHg
Storage
Store at 2-8°C
InChI
InChI=1S/C21H19NO4/c23-20(24)19(22-21(25)26-14-15-6-2-1-3-7-15)13-16-10-11-17-8-4-5-9-18(17)12-16/h1-12,19H,13-14H2,(H,22,25)(H,23,24)/t19-/m1/s1
InChI Key
XBRPIBMAJOTVHG-LJQANCHMSA-N
Canonical SMILES
C1=CC=C(C=C1)COC(=O)NC(CC2=CC3=CC=CC=C3C=C2)C(=O)O

Z-3-(2-naphthyl)-D-alanine, a chiral amino acid derivative, finds applications across diverse fields of bioscience. Here are the key applications presented with high perplexity and burstiness:

Pharmaceutical Development: Positioned at the forefront of pharmaceutical synthesis, Z-3-(2-naphthyl)-D-alanine plays a pivotal role in crafting pharmaceutical compounds especially those necessitating chiral purity. Acting as a foundational element for drug synthesis, it facilitates the creation of medications with precise stereochemistry thereby augmenting their pharmacological efficacy. Its intricate structure not only enables the exploration of novel therapeutic entities but also drives innovation in drug design promising enhanced pharmaceutical outcomes.

Peptide Synthesis: Embedding itself in the realm of peptide chemistry, this compound emerges as a valuable asset for generating peptides and peptidomimetics utilized in a myriad of research and therapeutic contexts. Integrating Z-3-(2-naphthyl)-D-alanine into peptide sequences enables manipulation of their biological functionality and resilience. By harnessing this compound's potential researchers can engineer cutting-edge peptides with heightened specificity and potency reshaping the landscape of peptide-based therapeutics.

Chiral Catalyst Development: Pioneering the domain of asymmetric synthesis, Z-3-(2-naphthyl)-D-alanine serves as a linchpin in crafting chiral catalysts pivotal for generating chiral molecules essential in diverse chemical and pharmaceutical processes. Infused with a chiral amino acid like Z-3-(2-naphthyl)-D-alanine these catalysts excel in achieving exceptional enantioselectivity in reactions underpinning the production of intricate molecular architectures and driving excellence in chemical synthesis.

Biochemical Research: Unveiling its prowess in biochemical investigations, Z-3-(2-naphthyl)-D-alanine emerges as a key tool for unraveling enzyme-substrate dynamics and protein conformation. By incorporating this amino acid into protein models researchers delve deep into the interplay of steric hindrance and electronic properties on enzyme functionality. This insightful exploration sheds light on the fundamental tenets of enzymatic catalysis and protein folding illuminating the intricacies of biochemical processes.

Online Inquiry
Verification code
Inquiry Basket