CAS 23239-35-2

2-Methyl-L-phenylalanine monohydrate

Description:

2-Methyl-L-phenylalanine monohydrate is an amino acid derivative characterized by its structural features, which include a methyl group attached to the alpha carbon of the phenylalanine backbone. This compound is a chiral molecule, existing in the L-form, which is biologically relevant and commonly found in proteins. The presence of the phenyl group contributes to its hydrophobic characteristics, while the amino and carboxyl functional groups confer its classification as an amino acid. As a monohydrate, it contains one molecule of water per molecule of the amino acid, which can influence its solubility and stability. This compound is often utilized in biochemical research and pharmaceutical applications, particularly in studies related to protein synthesis and enzyme activity. Its unique properties make it a valuable building block in peptide synthesis and in the development of novel therapeutic agents. Additionally, it may exhibit specific interactions with biological systems due to its structural similarities to naturally occurring amino acids.

Formula: C₁₀H₁₃NO₂

InChI: InChI=1S/C10H13NO2/c1-10(11,9(12)13)7-8-5-3-2-4-6-8/h2-6H,7,11H2,1H3,(H,12,13)/t10-/m0/s1

InChI key: InChIKey=HYOWVAAEQCNGLE-JTQLQIEISA-N

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

Synonyms:

• (2S)-2-Amino-2-methyl-3-phenylpropanoic acid
• (S)-(+)-2-Amino-2-methyl-3-phenylpropanoic acid monohydrate
• (S)-2-Amino-2-methyl-3-phenylpropanoicacid
• (S)-2-Methyl-3-phenylalanine
• (S)-2-Methylphenylalanine
• (S)-α-Methylphenylalanine
• <span class="text-smallcaps">L</span>-Phenylalanine, α-methyl-
• <span class="text-smallcaps">L</span>-α-Methylphenylalanine
• Alanine, 2-methyl-3-phenyl-, <span class="text-smallcaps">L</span>-
• L-a-Methylphenylalanine monohydrate
• α-Methyl-<span class="text-smallcaps">L</span>-phenylalanine
• α-Methyl-L-phenylalanine
• Alanine, 2-methyl-3-phenyl-, L-
• L-Phenylalanine, α-methyl-
• 2-Methyl-L-phenylalanine monohydrate
• ALPHA-ME-PHENYLALANINE
• -Benzyl-L-Ala
• H-ALPHA-ME-PHE-OH
• A-BENZYL-L-ALA
• ALPHA-BENZYL-L-ALA
• TIMTEC-BB SBB006742
• (S)-2-AMINO-2-METHYL-3-PHENYLPROPANOIC ACID
• H-(ME)PHE-OH
• (S)-(+)-2-AMINO-2-METHYL-3-PHENYLPROPANOIC ACID 1-HYDRATE (E.E.)
• ALPHA-METHYL-L-PHENYLALANINE
• (S)-a-Methyl-phenylalanine (>98%, >98%ee)
• H-ALPHA-ME-L-PHE-OH
• ALPHA-METHYL-L-PHE
• (S)-(+)-2-Amino-2-methyl-3-phenylpropanoicacidmonohydrate(e.e.)
• (S)-(+)-2-AMINO-2-METHYL-3-PHENYLPROPANOIC ACID
• (S)-(+)-2-AMINO-2-METHYL-3-PHENYLPROPANOIC ACID MONOHYDRATE, 99% (99+% E.E.)

L-Phenylalanine, α-methyl-

CAS: 23239-35-2

Formula: C₁₀H₁₃NO₂

Purity: 98%

Color and Shape: Solid

Molecular weight: 179.2157

Ref: IN-DA002MMX

(S)-2-Amino-2-methyl-3-phenylpropanoic acid

CAS: 23239-35-2

(S)-2-Amino-2-methyl-3-phenylpropanoic acid

Purity: 95%

Molecular weight: 179.22g/mol

Ref: 54-OR1032097

α-Methyl-L-phenylalanine

CAS: 23239-35-2

Formula: C₁₀H₁₃NO₂

Purity: ≥ 98.0%

Color and Shape: White to faint yellow powder

Molecular weight: 179.22

Ref: 7W-GC3493

α-Methyl-L-phenylalanine

Controlled Product

CAS: 23239-35-2

Applications α-Methyl-L-phenylalanine is used to prepare hippuryl-α-methylphenylalanine and hippuryl-α-methylphenyllactic acid as substrates for carboxypeptidase A. It is also used in the synthesis of high affinity tachykinin NK2 receptor antagonists.
References Lee, M., et al.: Bioorg. Med. Chem., 8, 815 (2000); Boyle, S., et al.: Bioorg. Med. Chem., 2, 101 (1994)

Formula: C₁₀H₁₃NO₂

Color and Shape: Neat

Molecular weight: 179.22

Ref: TR-M327145

(S)-2-Amino-2-methyl-3-phenylpropanoic acid

CAS: 23239-35-2

Formula: C₁₀H₁₃NO₂

Purity: 98%

Color and Shape: White powder

Molecular weight: 179.219

Ref: 10-F235494