119433-80-6 | L-4-Thiazolylalanine

Packsize	Purity	Availability	Price	Discounted Price
100mg	95%	in stock	$34.00	$24.00
250mg	95%	in stock	$60.00	$42.00
1g	95%	in stock	$65.00	$45.00
5g	95%	in stock	$188.00	$132.00
25g	95%	in stock	$829.00	$581.00

Description

• Catalog Number: AA24081
• Chemical Name: L-4-Thiazolylalanine
• CAS Number: 119433-80-6
• Molecular Formula: C6H8N2O2S
• Molecular Weight: 172.2049
• MDL Number: MFCD00079677
• SMILES: N[C@H](C(=O)O)Cc1cscn1

Computed Properties

• Complexity: 154
• Covalently-Bonded Unit Count: 1
• Defined Atom Stereocenter Count: 1
• Heavy Atom Count: 11
• Hydrogen Bond Acceptor Count: 5
• Hydrogen Bond Donor Count: 2
• Rotatable Bond Count: 3
• XLogP3: -2.3

Upstream Synthesis Route

3-(4-Thiazolyl)-L-alanine is a valuable compound widely used in chemical synthesis as a versatile building block. Its unique structure, incorporating a thiazole ring and an amino acid moiety, offers a range of potential applications in the field of organic chemistry.One key application of 3-(4-Thiazolyl)-L-alanine is its use as a chiral ligand in asymmetric catalysis. The presence of the thiazole ring imparts additional stereoelectronic effects, which can enhance the enantioselectivity of certain catalytic reactions. This makes it a valuable tool for synthesizing chiral compounds with high optical purity, important in the pharmaceutical and agrochemical industries.Furthermore, 3-(4-Thiazolyl)-L-alanine can serve as a precursor for the synthesis of various biologically active molecules. By selectively modifying different functional groups on the molecule, chemists can access a diverse array of analogs with potentially enhanced pharmacological properties. This versatility makes it a valuable starting material for drug discovery efforts and medicinal chemistry research.In addition, the thiazole ring in 3-(4-Thiazolyl)-L-alanine can undergo various functionalization reactions, allowing for the introduction of different substituents and functionalities. This flexibility enables the synthesis of novel compounds with tailored properties for specific applications, ranging from materials science to chemical biology.Overall, the unique structure and reactivity of 3-(4-Thiazolyl)-L-alanine make it an invaluable tool in chemical synthesis, with broad applications in asymmetric catalysis, drug discovery, and materials science.