Cas no 19789-59-4 (2-Amino-2-(4-methoxyphenyl)acetic acid)

2-Amino-2-(4-methoxyphenyl)acetic acid is a chiral α-amino acid derivative featuring a 4-methoxyphenyl substituent, which imparts unique steric and electronic properties. This compound is valuable as a building block in organic synthesis, particularly for the preparation of pharmaceuticals, peptidomimetics, and fine chemicals. The presence of both amino and carboxyl functional groups allows for versatile reactivity, enabling incorporation into more complex molecular frameworks. Its methoxy group enhances solubility in organic solvents and may influence biological activity. The compound is often utilized in asymmetric synthesis and medicinal chemistry research due to its potential as a precursor for bioactive molecules. Proper handling under controlled conditions is recommended due to its reactivity.
2-Amino-2-(4-methoxyphenyl)acetic acid structure
19789-59-4 structure
Product Name:2-Amino-2-(4-methoxyphenyl)acetic acid
CAS No:19789-59-4
MF:C9H11NO3
MW:181.188542604446
MDL:MFCD00049329
CID:158516
PubChem ID:265442
Update Time:2025-11-06

2-Amino-2-(4-methoxyphenyl)acetic acid Chemical and Physical Properties

Names and Identifiers

    • 2-Amino-2-(4-methoxyphenyl)acetic acid
    • α-Aminohomoanisic acid
    • (?à)-4-METHOXYPHENYL GLYCIN
    • DL-4-methoxyphenyl glycine
    • ()-4-METHOXYPHENYL GLYCIN
    • 4-METHOXY PHENYLGLYCINE
    • a-Amino-4-methoxybenzeneacetic acid
    • AMINO(4-METHOXYPHENYL)ACETIC ACID
    • Benzeneacetic acid,a-aMino-4-Methoxy
    • N-(4-METHOXYPHENYL)-GLYCINE
    • 2-Amino-2-(4-methoxyphenyl)ethanoic acid
    • DL-p-Methoxyphenylglycine
    • NSC 101476
    • NSC 154924
    • dl-2-(p-Methoxyphenyl)glycine
    • alpha-Aminohomoanisic acid
    • BIO-FARMA BF000291
    • RS-4-methoxyphenylglycine
    • 2-AMino-2-(4-Methoxypheny...
    • ( inverted exclamation markA)-4-Methoxyphenyl glycine
    • 2-Amino-2-(4-methoxyphenyl)aceticAcid
    • Benzeneacetic acid, alpha-amino-4-methoxy-
    • NSC154924
    • 2-(4-Methoxyphenyl)glycine
    • (+/-)-4-Methoxyphenyl glycine
    • GXUAKXUIILGDKW-UHFFFAOYSA-N
    • HMS1787F01
    • BBL022157
    • STK131290
    • 0184AB
    • AKOS000182859
    • BB 0249635
    • 19789-59-4
    • SY014170
    • CHEMBL134005
    • L-4-METHOXYPHENYLGLYCINE
    • SCHEMBL5281443
    • NSC101476
    • 6L-303S
    • CS-0030788
    • Amino-(4-methoxy-phenyl)-acetic acid
    • FT-0637909
    • NSC 101476; NSC 154924
    • AKOS016053343
    • PB10070
    • EN300-69643
    • AB32874
    • -Aminohomoanisic acid
    • AMY9093
    • AB32877
    • 2540-53-6
    • Z56755722
    • MFCD00049329
    • D-28
    • F2167-0082
    • Benzeneacetic acid, a-amino-4-methoxy-
    • NSC-101476
    • AC-23606
    • NSC-154924
    • AMINO-4-METHOXYBEN-ZENEACETIC ACID
    • DB-044988
    • MDL: MFCD00049329
    • Inchi: 1S/C9H11NO3/c1-13-7-4-2-6(3-5-7)8(10)9(11)12/h2-5,8H,10H2,1H3,(H,11,12)
    • InChI Key: GXUAKXUIILGDKW-UHFFFAOYSA-N
    • SMILES: O(C)C1C=CC(=CC=1)C(C(=O)O)N

Computed Properties

  • Exact Mass: 181.07400
  • Monoisotopic Mass: 181.074
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 2
  • Hydrogen Bond Acceptor Count: 4
  • Heavy Atom Count: 13
  • Rotatable Bond Count: 3
  • Complexity: 176
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 1
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • Surface Charge: 0
  • Tautomer Count: nothing
  • XLogP3: -1.7
  • Topological Polar Surface Area: 72.6

Experimental Properties

  • Density: 1.246±0.06 g/cm3 (20 oC 760 Torr),
  • Melting Point: 284-285 °C (decomposition)
  • Boiling Point: 339.5℃ at 760 mmHg
  • Flash Point: 159.1℃
  • Refractive Index: 1.568
  • Solubility: Slightly soluble (18 g/l) (25 o C),
  • PSA: 72.55000
  • LogP: 1.47990

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2-Amino-2-(4-methoxyphenyl)acetic acid Related Literature

Additional information on 2-Amino-2-(4-methoxyphenyl)acetic acid

Market Research and Analysis Report on 2-Amino-2-(4-Methoxyphenyl)Acetic Acid (CAS No. 19789-59-4)

2-Amino-2-(4-methoxyphenyl)acetic acid, identified by the CAS number 19789-59-4, is a compound of significant interest in the chemical, biotechnological, and pharmaceutical industries. This report provides an in-depth analysis of the latest research findings, market demands, and supply chain dynamics surrounding this compound.

The compound has been extensively studied for its potential applications in drug development, particularly in the field of oncology. Recent studies have highlighted its role as a precursor in the synthesis of certain anticancer agents. Its unique chemical structure, featuring an amino group and a methoxy-substituted phenyl ring, contributes to its versatility in various synthetic pathways.

Market demand for 2-Amino-2-(4-methoxyphenyl)acetic acid has been driven by increasing investments in research and development activities within the pharmaceutical sector. The growing focus on personalized medicine and targeted therapies has further amplified the need for high-quality raw materials like this compound. Key regions exhibiting strong demand include North America, Europe, and Asia-Pacific, with emerging markets showing promising growth potential.

From a supply perspective, several global chemical manufacturers specialize in the production of this compound. These suppliers adhere to stringent quality control measures to ensure compliance with international standards. The competitive landscape is characterized by both established players and emerging suppliers striving to meet the evolving needs of their clients.

Research methodologies employed in this analysis include comprehensive literature reviews of peer-reviewed journals, industry reports, and market intelligence databases. Data collection was supplemented by interviews with industry experts and key opinion leaders to gather insights into current trends and future projections.

The findings underscore the critical role of 2-Amino-2-(4-methoxyphenyl)acetic acid in advancing therapeutic innovations. As the demand for specialized chemical intermediates continues to rise, stakeholders are encouraged to invest in robust supply chain strategies to maintain a competitive edge.

In conclusion, this report serves as a valuable resource for professionals involved in the development, manufacturing, and procurement of chemical intermediates within the biopharmaceutical sector. By leveraging cutting-edge research and market insights, organizations can better navigate the complexities of this dynamic industry.

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