Boc-β-(2-thienyl)-L-alanine
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Boc-β-(2-thienyl)-L-alanine

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Category
BOC-Amino Acids
Catalog number
BAT-007180
CAS number
56675-37-7
Molecular Formula
C12H17NO4S
Molecular Weight
271.33
Boc-β-(2-thienyl)-L-alanine
IUPAC Name
(2S)-2-[(2-methylpropan-2-yl)oxycarbonylamino]-3-thiophen-2-ylpropanoic acid
Synonyms
Boc-3-L-Ala(2-thienyl)-OH; (S)-N-Boc-2-thienylalanine
Related CAS
78512-39-7 (DL-isomer)
Appearance
White powder
Purity
≥ 98% (HPLC)
Density
1.243 g/cm3
Melting Point
71-76 °C
Boiling Point
431.5 °C at 760 mmHg
Storage
Store at 2-8 °C
InChI
InChI=1S/C12H17NO4S/c1-12(2,3)17-11(16)13-9(10(14)15)7-8-5-4-6-18-8/h4-6,9H,7H2,1-3H3,(H,13,16)(H,14,15)/t9-/m0/s1
InChI Key
OJLISTAWQHSIHL-VIFPVBQESA-N
Canonical SMILES
CC(C)(C)OC(=O)NC(CC1=CC=CS1)C(=O)O

Boc-β-(2-thienyl)-L-alanine, an amino acid derivative, highly utilized in peptide synthesis and diverse research endeavors. Here are the key applications presented with a high degree of perplexity and burstiness:

Peptide Synthesis: An invaluable tool in crafting intricate peptides and proteins, Boc-β-(2-thienyl)-L-alanine's distinctive side chain infuses peptides with thienyl functionality enabling the exploration of protein structure and function. This compound plays a pivotal role in tailoring peptides with specific biological and chemical traits potentially heralding the dawn of groundbreaking therapeutic entities.

Medicinal Chemistry: In the realm of drug design, Boc-β-(2-thienyl)-L-alanine serves as a foundational element for synthesizing bioactive compounds. Its integration into drug candidates can augment target interactions enhancing binding specificity and refining the pharmacological characteristics of novel therapeutics. Researchers actively explore its potential in creating fresh inhibitors or stimulators of biological pathways pushing the boundaries of pharmaceutical innovation.

Chemical Biology: Acting as a cornerstone in chemical biology, Boc-β-(2-thienyl)-L-alanine illuminates protein interactions and signaling pathways. By incorporating this amino acid derivative into peptides, scientists delve into the impact of specific residues on protein functions unraveling intricate molecular mechanisms and pinpointing potential therapeutic targets. This meticulous exploration aids in deciphering the complexities of biological systems and charting new avenues for therapeutic interventions.

Material Science: At the intersection of science and innovation, Boc-β-(2-thienyl)-L-alanine finds its place in crafting novel biomaterials. Its unique attributes enable the development of surfaces and materials tailored for specific interactions with biological entities paving the way for advanced biomaterials used in biomedical applications like drug delivery systems and tissue engineering scaffolds. This application stands as a testament to the boundless possibilities of integrating molecular design with material science shaping the future of biomedical engineering.

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