CAS 10172-89-1

(-)-N-Acetylphenylalanine

Description:

(-)-N-Acetylphenylalanine, with the CAS number 10172-89-1, is an amino acid derivative characterized by the presence of an acetyl group attached to the nitrogen of the phenylalanine side chain. This compound is a chiral molecule, existing in two enantiomeric forms, with the (-) designation indicating its specific stereochemistry. It is typically a white to off-white crystalline solid that is soluble in polar solvents such as water and methanol, reflecting its polar nature due to the amino and acetyl functional groups. The compound is often utilized in biochemical research and pharmaceutical applications, particularly in studies involving protein synthesis and enzyme activity, due to its structural similarity to natural amino acids. Its acetylation can influence the compound's reactivity and interaction with biological systems, making it a valuable tool in medicinal chemistry and drug design. Additionally, (-)-N-Acetylphenylalanine may exhibit specific biological activities, although detailed studies are necessary to elucidate its full range of effects.

Formula: C₁₁H₁₃NO₃

InChI: InChI=1S/C11H13NO3/c1-8(13)12-10(11(14)15)7-9-5-3-2-4-6-9/h2-6,10H,7H2,1H3,(H,12,13)(H,14,15)/t10-/m1/s1

InChI key: InChIKey=CBQJSKKFNMDLON-SNVBAGLBSA-N

SMILES: [C@H](CC1=CC=CC=C1)(NC(C)=O)C(O)=O

Synonyms:

• (-)-2-Acetylamino-3-phenylpropanoic acid
• (-)-N-Acetyl-<span class="text-smallcaps">D</span>-phenylalanine
• (-)-N-Acetylphenylalanine
• (2R)-2-Acetamido-3-phenylpropanoic acid
• (R)-(-)-N-Acetylphenylalanine
• (R)-2-Acetamido-3-phenylpropanoic acid
• (R)-2-Acetylamino-3-phenylpropionic acid
• <span class="text-smallcaps">D</span>-(-)-N-Acetylphenylalanine
• <span class="text-smallcaps">D</span>-Phenylalanine, N-acetyl-
• Ac-D-Phe-OH
• Acetyl-D-Phenylalanine
• Acetylphenylalanine
• Alanine, N-acetyl-3-phenyl-, <span class="text-smallcaps">D</span>-
• N-Acetyl-(R)-phenylalanine
• N-Acetyl-3-phenyl-<span class="text-smallcaps">D</span>-alanine
• NSC 523830
• R-2-(Acetylamino)-3-phenylpropanoic acid
• D-Phenylalanine, N-acetyl-
• N-Acetyl-D-phenylalanine

D-Phenylalanine, N-acetyl-

CAS: 10172-89-1

Formula: C₁₁H₁₃NO₃

Purity: 95%

Color and Shape: Solid

Molecular weight: 207.2258

Ref: IN-DA0005B8

N-Acetyl-D-Phenylalanine

CAS: 10172-89-1

N-Acetyl-D-Phenylalanine

Purity: 98%

Molecular weight: 207.23g/mol

Ref: 54-OR1014233

N-Acetyl-D-phenylalanine

CAS: 10172-89-1

Formula: C₁₁H₁₃NO₃

Purity: >98.0%(T)(HPLC)

Color and Shape: White powder to crystal

Molecular weight: 207.23

Ref: 3B-A0105

N-Acetyl-D-phenylalanine

CAS: 10172-89-1

Formula: C₁₁H₁₃NO₃

Purity: 95%

Color and Shape: Solid

Molecular weight: 207.229

Ref: 10-F092214

N-Acetyl-D-phenylalanine

Controlled Product

CAS: 10172-89-1

Applications Protected amino acid.
References Zhang, T., et al.: J. Pharm. Biomed. Anal., 46, 882 (2008), Cummings, J., et al.: Biochem., 48, 6469 (2009),

Formula: C₁₁H₁₃NO₃

Color and Shape: Neat

Molecular weight: 207.23

Ref: TR-A187380

N-Acetyl-D-phenylalanine

CAS: 10172-89-1

N-Acetyl-D-phenylalanine is a synthetic amino acid that is used as a building block in the synthesis of peptides and proteins. It is produced by the Friedel-Crafts reaction between benzene and acetic anhydride, which results in formation of the molecule with two phenyl groups. N-Acetyl-D-phenylalanine has been shown to react with water molecules to form supramolecular complexes, which may be immobilized for use as catalysts for chemical reactions. The rate of this reaction depends on the concentration of carbon source and substrate concentration.

Formula: C₁₁H₁₃NO₃

Purity: Min. 95%

Molecular weight: 207.23 g/mol

Ref: 3D-FA17118