Cas no 119397-07-8 (Benzeneacetic acid, a-amino-3-methyl-, (aS)-)

Benzeneacetic acid, α-amino-3-methyl-, (αS)-, is a chiral aromatic amino acid derivative characterized by its stereospecific configuration at the α-carbon. This compound is of interest in synthetic organic chemistry and pharmaceutical research due to its structural features, which include a benzene ring and a methyl-substituted amino acid moiety. The (αS)-enantiomer offers precise stereochemical control in asymmetric synthesis, making it valuable for the development of enantiomerically pure intermediates or active pharmaceutical ingredients (APIs). Its stability and well-defined chirality also facilitate applications in peptide modification and ligand design. The compound is typically handled under standard laboratory conditions, with attention to its reactivity and solubility profile.
Benzeneacetic acid, a-amino-3-methyl-, (aS)- structure
119397-07-8 structure
Product Name:Benzeneacetic acid, a-amino-3-methyl-, (aS)-
CAS No:119397-07-8
MF:C9H11NO2
MW:165.189142465591
MDL:MFCD07371677
CID:133067
PubChem ID:7022634
Update Time:2025-06-08

Benzeneacetic acid, a-amino-3-methyl-, (aS)- Chemical and Physical Properties

Names and Identifiers

    • Benzeneacetic acid, a-amino-3-methyl-, (aS)-
    • (2S)-2-amino-2-(3-methylphenyl)acetic acid
    • (S)?-Α-?AMINO-?3-?METHYL-BENZENEACETIC ACID
    • 3-METHYL-L-PHENYLGLYCINE
    • S-3-Methylphenylglycine
    • (S)-a-AMino-3-Methyl-benzeneacetic acid
    • (S)-2-amino-2-(3-methylphenyl)acetic acid
    • Benzeneacetic acid, alpha-amino-3-methyl-, (alphaS)- (9CI)
    • Benzeneacetic acid,alpha-amino-3-methyl-,(alphas)-(9ci)
    • (S)-2-Amino-2-(m-tolyl)aceticacid
    • CS-0363187
    • (alphaS)-alpha-Amino-3-methylbenzeneacetic acid
    • N15140
    • DTXSID301281012
    • 119397-07-8
    • (S)-2-Amino-2-(m-tolyl)acetic acid
    • AS-77821
    • (S)-alpha-Amino-3-methyl-benzeneacetic acid
    • MDL： MFCD07371677
    • Inchi： 1S/C9H11NO2/c1-6-3-2-4-7(5-6)8(10)9(11)12/h2-5,8H,10H2,1H3,(H,11,12)/t8-/m0/s1
    • InChI Key： LUSUJXIQPCPYCT-QMMMGPOBSA-N
    • SMILES： OC([C@H](C1C=CC=C(C)C=1)N)=O

Computed Properties

  • Exact Mass: 272.08309
  • Monoisotopic Mass: 165.078978594g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 2
  • Hydrogen Bond Acceptor Count: 3
  • Heavy Atom Count: 12
  • Rotatable Bond Count: 2
  • Complexity: 170
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 1
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • XLogP3: -1.3
  • Topological Polar Surface Area: 63.3?2

Experimental Properties

  • PSA: 52.54

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Benzeneacetic acid, a-amino-3-methyl-, (aS)- Suppliers

Amadis Chemical Company Limited
Gold Member
Audited Supplier Audited Supplier
(CAS:119397-07-8)Benzeneacetic acid, a-amino-3-methyl-, (aS)-
Order Number:A931820
Stock Status:in Stock
Quantity:1g/5g
Purity:99%
Pricing Information Last Updated:Friday, 30 August 2024 15:06
Price ($):162.0/597.0

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Additional information on Benzeneacetic acid, a-amino-3-methyl-, (aS)-

Comprehensive Overview of Benzeneacetic acid, a-amino-3-methyl-, (aS)- (CAS No. 119397-07-8): Properties, Applications, and Research Insights

Benzeneacetic acid, a-amino-3-methyl-, (aS)- (CAS No. 119397-07-8) is a chiral organic compound with significant relevance in pharmaceutical and biochemical research. This optically active derivative of benzeneacetic acid features an amino group and a methyl substituent at the alpha position, making it a valuable intermediate in asymmetric synthesis. Its stereospecificity and molecular structure have attracted attention for applications in drug development, particularly in designing enzyme inhibitors and peptide mimetics.

The compound’s chiral purity (denoted by the (aS)- configuration) is critical for its biological activity, aligning with the growing demand for enantioselective synthesis in modern medicinal chemistry. Researchers frequently explore its role in structure-activity relationship (SAR) studies, where subtle modifications to its scaffold can yield compounds with enhanced selectivity or potency. Recent trends in green chemistry have also spurred interest in eco-friendly synthesis routes for such intermediates, reducing reliance on hazardous reagents.

In the context of user search trends, queries like "chiral building blocks for drug discovery" or "CAS 119397-07-8 applications" reflect the compound’s niche yet expanding relevance. Analytical techniques such as HPLC and NMR are often employed to verify its purity, a topic frequently searched by quality control professionals. Additionally, discussions on patent literature around similar structures highlight its potential in proprietary formulations.

From a regulatory perspective, Benzeneacetic acid, a-amino-3-methyl-, (aS)- is not classified as hazardous under major chemical inventories, though standard laboratory safety protocols apply. Its stability under ambient conditions makes it suitable for long-term storage, a practical advantage for industrial users. As the pharmaceutical industry shifts toward personalized medicine, the demand for chiral intermediates like this compound is projected to rise, driven by their role in creating targeted therapies.

Future research may explore its utility in biocatalysis or computational drug design, areas gaining traction in academic and industrial circles. For those sourcing the compound, verifying supplier certifications and technical data sheets remains essential, as emphasized in SEO-optimized procurement guides. This aligns with broader industry priorities like supply chain transparency and sustainable sourcing.

119397-07-8 (Benzeneacetic acid, a-amino-3-methyl-, (aS)-) Related Products

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Amadis Chemical Company Limited
(CAS:119397-07-8)Benzeneacetic acid, a-amino-3-methyl-, (aS)-
A931820
Purity:99%/99%
Quantity:1g/5g
Price ($):162.0/597.0
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