1012-05-1 | DL-Homophenylalanine

Packsize	Purity	Availability	Price	Discounted Price
5g	98%	in stock	$21.00	$15.00
10g	98%	in stock	$26.00	$18.00
25g	98%	in stock	$62.00	$44.00
100g	98%	in stock	$156.00	$109.00

Description

• Catalog Number: AA04911
• Chemical Name: DL-Homophenylalanine
• CAS Number: 1012-05-1
• Molecular Formula: C10H13NO2
• Molecular Weight: 179.2157
• MDL Number: MFCD00063092
• SMILES: NC(C(=O)O)CCc1ccccc1

Computed Properties

• Complexity: 164
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 13
• Hydrogen Bond Acceptor Count: 3
• Hydrogen Bond Donor Count: 2
• Rotatable Bond Count: 4
• Undefined Atom Stereocenter Count: 1
• XLogP3: -1.2

Upstream Synthesis Route

H-DL-HoPhe-OH is a versatile amino acid derivative that finds widespread applications in chemical synthesis. It serves as a key building block in peptide synthesis, where it can be incorporated into peptide chains to introduce specific structural and functional properties. Due to its unique chemical structure, H-DL-HoPhe-OH enables chemists to create customized peptide sequences with enhanced stability, bioactivity, or binding properties.In organic chemistry, H-DL-HoPhe-OH is utilized for the preparation of various peptidomimetics and drug molecules. Its presence in the peptide backbone can influence the secondary structure and overall conformational stability of the resulting molecules, making it a valuable tool for drug design and discovery. Additionally, H-DL-HoPhe-OH can be used in the synthesis of complex natural products, where its incorporation can impart desired biological activities or improve pharmacokinetic properties.Furthermore, H-DL-HoPhe-OH plays a crucial role in the study of protein structure and function. By incorporating this amino acid derivative into peptides or proteins, researchers can probe specific interactions, folding patterns, and molecular recognition events. This aids in the elucidation of biological mechanisms, protein-protein interactions, and drug-target binding, leading to valuable insights for drug development and biochemical research.

Literature

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