1142-20-7 | Z-Ala-OH

Packsize	Purity	Availability	Price	Discounted Price
250mg	95%	in stock	$15.00	$10.00
1g	95%	in stock	$16.00	$11.00
5g	95%	in stock	$18.00	$12.00
25g	95%	in stock	$28.00	$19.00
100g	95%	in stock	$62.00	$44.00
250g	95%	in stock	$135.00	$94.00
500g	95%	in stock	$180.00	$126.00

Description

• Catalog Number: AB77202
• Chemical Name: Z-Ala-OH
• CAS Number: 1142-20-7
• Molecular Formula: C11H13NO4
• Molecular Weight: 223.2252
• MDL Number: MFCD00002640
• SMILES: C[C@@H](C(=O)O)NC(=O)OCc1ccccc1

Computed Properties

• Complexity: 248
• Covalently-Bonded Unit Count: 1
• Defined Atom Stereocenter Count: 1
• Heavy Atom Count: 16
• Hydrogen Bond Acceptor Count: 4
• Hydrogen Bond Donor Count: 2
• Rotatable Bond Count: 5
• XLogP3: 1.4

Upstream Synthesis Route

N-[(Phenylmethoxy)carbonyl]-L-alanine serves as a versatile building block in chemical synthesis, specifically in peptide and pharmaceutical industries. This compound is commonly used as a protecting group for the amino acid alanine due to its stability and easy removal under mild conditions. By selectively shielding the amine group of alanine with N-[(Phenylmethoxy)carbonyl], chemists can prevent unwanted reactions during peptide chain assembly and ensure the precise incorporation of alanine into the desired peptide sequence. Additionally, the presence of the phenylmethoxy carbonyl moiety provides a strategic handle for further functional group manipulations, allowing for the synthesis of complex and diverse peptide structures. Its compatibility with a wide range of reagents and conditions makes N-[(Phenylmethoxy)carbonyl]-L-alanine a valuable tool for the efficient and controlled synthesis of peptides and pharmaceutical compounds.

Literature

• Rational nanoconjugation improves biocatalytic performance of enzymes: aldol addition catalyzed by immobilized rhamnulose-1-phosphate aldolase.

  Langmuir : the ACS journal of surfaces and colloids 20120417

• Function and biotechnology of extremophilic enzymes in low water activity.

  Aquatic biosystems 20120101

• Highly active metallocarboxypeptidase from newly isolated Geobacillus strain SBS-4S: cloning and characterization.

  Journal of bioscience and bioengineering 20110301

• Design and synthesis of a tetradentate '3-amine-1-carboxylate' ligand to mimic the metal binding environment at the non-heme iron(II) oxidase active site.

  Organic & biomolecular chemistry 20100407

• Eutectic formation analysis of amino acid mixtures using molecular dynamics simulations.

  Biotechnology progress 20050101