119434-75-2 | Boc-L-4-thiazolylalanine

Packsize	Purity	Availability	Price	Discounted Price
250mg	97%	in stock	$34.00	$24.00
1g	97%	in stock	$60.00	$42.00
25g	97%	in stock	$1,073.00	$751.00

Description

• Catalog Number: AA24126
• Chemical Name: Boc-L-4-thiazolylalanine
• CAS Number: 119434-75-2
• Molecular Formula: C11H16N2O4S
• Molecular Weight: 272.3207
• MDL Number: MFCD00079682
• SMILES: O=C(OC(C)(C)C)N[C@H](C(=O)O)Cc1ncsc1

Upstream Synthesis Route

(S)-2-((tert-Butoxycarbonyl)amino)-3-(thiazol-4-yl)propanoic acid, commonly referred to as $name$, is a versatile compound extensively utilized in chemical synthesis processes. It serves as a critical building block in the creation of various biologically active molecules and pharmaceuticals. Specifically, this compound is highly valued in peptide synthesis due to its ability to act as a protected amino acid derivative.In peptide synthesis, (S)-2-((tert-Butoxycarbonyl)amino)-3-(thiazol-4-yl)propanoic acid functions as an essential intermediate for the formation of peptidyl thioesters. These thioesters are crucial intermediates in the assembly of peptides and proteins, facilitating controlled peptide bond formation and subsequent coupling reactions. Moreover, the tert-butoxycarbonyl (Boc) protecting group on the amino functionality of the compound plays a key role in shielding the amine group during peptide assembly, enabling selective deprotection and manipulation of the peptide sequence.Overall, the application of (S)-2-((tert-Butoxycarbonyl)amino)-3-(thiazol-4-yl)propanoic acid in chemical synthesis underscores its significance in peptide chemistry and drug development, highlighting its utility as a fundamental component in the construction of complex peptide structures with tailored biological activities.