CAS 943-73-7

L-Homophenylalanine

Description:

L-Homophenylalanine is an amino acid derivative that is structurally related to phenylalanine, featuring a homophenyl group in its side chain. It is classified as a non-polar, aliphatic amino acid due to the presence of a phenyl group, which contributes to its hydrophobic characteristics. This compound is often utilized in biochemical research and pharmaceutical applications, particularly in the synthesis of peptides and proteins. L-Homophenylalanine can participate in various biochemical reactions, including those involving enzyme catalysis and protein folding. Its CAS number, 943-73-7, is a unique identifier that facilitates the identification and study of this compound in scientific literature and databases. The substance is typically available in a crystalline form and is soluble in water, making it suitable for various laboratory applications. As with many amino acids, it plays a role in metabolic pathways and can influence the synthesis of neurotransmitters and other biologically significant molecules. Safety data should be consulted for handling and usage, as with all chemical substances.

Formula: C₁₀H₁₃NO₂

InChI: InChI=1S/C10H13NO2/c11-9(10(12)13)7-6-8-4-2-1-3-5-8/h1-5,9H,6-7,11H2,(H,12,13)/t9-/m0/s1

InChI key: InChIKey=JTTHKOPSMAVJFE-VIFPVBQESA-N

SMILES: C(C[C@@H](C(O)=O)N)C1=CC=CC=C1

Synonyms:

• (+)-2-Amino-4-Phenylbutyric Acid
• (+)-<span class="text-smallcaps">L</span>-Homophenylalanine
• (+)-Homophenylalanine
• (2S)-2-Amino-4-phenylbutanoic acid
• (2S)-2-Azaniumyl-4-phenylbutanoate
• (S)-(+)-2-Amino-4-Phenylbutyric Acid
• (S)-2-Amino-4-Phenylbutanoic Acid
• (S)-Alpha-Aminobenzenebutanoic Acid
• (S)-Homophenylalanine
• (S)-alpha-Amino-benzenebutanoic acid
• (αS)-α-Aminobenzenebutanoic acid
• 2-(S)-Amino-4-Phenylbutanoic Acid
• 2-Amino-4-Phenylbutanoic Acid
• <span class="text-smallcaps">L</span>-2-Amino-4-phenylbutyric acid
• <span class="text-smallcaps">L</span>-Benzylalanine
• <span class="text-smallcaps">L</span>-γ-Phenylbutyrine
• Benzenebutanoic acid, α-amino-, (S)-
• Benzenebutanoic acid, α-amino-, (αS)-
• Butyric acid, 2-amino-4-phenyl-, <span class="text-smallcaps">L</span>-
• H-HoPhe-OH
• Rarechem Bk Pt 0049
• Butyric acid, 2-amino-4-phenyl-, L-

L-Homophenylalanine, 98%

CAS: 943-73-7

L-Homophenylalanine is used as a precursor in the pharmaceutical industry for the production of angiotensin-converting enzyme (ACE) and R-(-)-Homophenylalanin-ethylester. It is also involved in the synthesis of NEPA [(S,S)-N-(1-Ethoxycarbonyl-3-phenylpropyl)alanine], which is a key intermediate to p

Formula: C₁₀H₁₃NO₂

Purity: 98%

Color and Shape: White, Powder

Molecular weight: 179.22

Ref: 02-H27295

H-Homophe-OH

CAS: 943-73-7

Bachem ID: 4005372.

Formula: C₁₀H₁₃NO₂

Purity: > 99%

Color and Shape: White

Molecular weight: 179.22

Ref: 01-4005372

(S)-2-Amino-4-Phenylbutyric Acid

CAS: 943-73-7

Formula: C₁₀H₁₃NO₂

Purity: 98%

Color and Shape: Solid

Molecular weight: 179.2157

Ref: IN-DA0032GV

L-Homophenylalanine

CAS: 943-73-7

L-Homophenylalanine

Purity: 98%

Molecular weight: 179.22g/mol

Ref: 54-OR14697

L-Homophenylalanine

CAS: 943-73-7

Formula: C₁₀H₁₃NO₂

Molecular weight: 179.22

Ref: 7W-GM7560

L-Homophenylalanine

CAS: 943-73-7

Formula: C₁₀H₁₃NO₂

Purity: >98.0%(T)

Color and Shape: White to Almost white powder to crystal

Molecular weight: 179.22

Ref: 3B-H0985

(L)-Homophenylalanine

CAS: 943-73-7

Formula: C₁₀H₁₃NO₂

Purity: 98%

Color and Shape: Solid, Powder

Molecular weight: 179.219

Ref: 10-F011758

L-Homophenylalanine extrapure, 97%

CAS: 943-73-7

Formula: C₁₀H₁₃NO₂

Purity: min. 97%

Color and Shape: White, Crystalline powder

Molecular weight: 179.22

Ref: SR-78523

L-Homophenylalanine

Controlled Product

CAS: 943-73-7

Applications Antitumor agent.
References Brunner, Henri., et al.: Eur. J. Med. Chem., 25, 35 (1990),

Formula: C₁₀H₁₃NO₂

Color and Shape: Neat

Molecular weight: 179.22

Ref: TR-H600500