Boc-β-chloro-L-alanine
Need Assistance?
  • US & Canada:
    +
  • UK: +

Boc-β-chloro-L-alanine

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

Category
BOC-Amino Acids
Catalog number
BAT-007182
CAS number
71404-98-3
Molecular Formula
C8H14NO4Cl
Molecular Weight
223.65
Boc-β-chloro-L-alanine
IUPAC Name
(2R)-3-chloro-2-[(2-methylpropan-2-yl)oxycarbonylamino]propanoic acid
Synonyms
Boc-β-chloro-L-Ala-OH; Boc-3-Chloro-L-alanine
Appearance
White to off-white powder
Purity
≥ 95% (NMR)
Storage
Store at 2-8 °C
InChI
InChI=1S/C8H14ClNO4/c1-8(2,3)14-7(13)10-5(4-9)6(11)12/h5H,4H2,1-3H3,(H,10,13)(H,11,12)/t5-/m0/s1
InChI Key
NMRCVEILBKVWIK-YFKPBYRVSA-N
Canonical SMILES
CC(C)(C)OC(=O)NC(CCl)C(=O)O

Boc-β-chloro-L-alanine, a chemically modified amino acid, finds applications primarily in synthetic chemistry and biochemical research. Here are the key applications explained with high perplexity and burstiness:

Peptide Synthesis: Playing a pivotal role in peptide synthesis, Boc-β-chloro-L-alanine acts as a fundamental building block in creating diverse synthetic peptides. Its shielded amino group (Boc) shields against undesired side reactions during peptide bond formation enabling precise assembly of peptide chains with customized sequences and attributes.

Enzyme Inhibitor Development: Instrumental in crafting enzyme inhibitors especially those targeting amino acid-interacting enzymes, Boc-β-chloro-L-alanine is essential for designing compounds that tightly and selectively bind to specific enzymes. This strategic incorporation aids in deciphering enzyme mechanisms and advancing therapeutic agent development.

Protease Studies: In protease investigations, scientists utilize Boc-β-chloro-L-alanine to study enzymes that cleave peptide bonds. By integrating this compound into substrates, researchers generate protease-resistant peptide sequences facilitating the exploration of protease specificity and activity offering insights into enzyme functionality and potential drug targets.

Protein Structure-Activity Relationship (SAR) Analysis: Applied in SAR investigations, Boc-β-chloro-L-alanine aids in unraveling the intricate link between protein structure and biological activity. Substituting amino acids with this modified variant allows researchers to observe alterations in protein function and stability crucial for rational drug design and protein engineering endeavors.

Online Inquiry
Verification code
Inquiry Basket