• 1. Forchlorfenuron-mimicking haptens: from immunogen design to antibody characterization by hierarchical clustering analysis
  Celia Suárez-Pantaleón,Josep V. Mercader,Consuelo Agulló,Antonio Abad-Somovilla,Antonio Abad-Fuentes Org. Biomol. Chem. 2011 9 4863
• 2. 2-Arylamino-6-ethynylpurines are cysteine-targeting irreversible inhibitors of Nek2 kinase
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• Solvents and Organic Chemicals Organic Compounds Benzenoids Benzene and substituted derivatives Aniline and substituted anilines
• Solvents and Organic Chemicals Organic Compounds Acids/Esters

Exploring the Versatile Applications and Properties of 2-(3-Aminophenyl)acetic Acid (CAS No. 14338-36-4)

2-(3-Aminophenyl)acetic acid, with the CAS number 14338-36-4, is a significant organic compound widely recognized in pharmaceutical and chemical research. This aromatic amino acid derivative is characterized by its amino group and carboxylic acid functionality, making it a valuable intermediate in the synthesis of various bioactive molecules. Researchers and industries often search for 2-(3-aminophenyl)acetic acid uses, synthesis methods, and suppliers, reflecting its growing importance in modern chemistry.

The compound's molecular formula is C₈H₉NO₂, and it exhibits a molecular weight of 151.16 g/mol. Its structure consists of a phenyl ring substituted with an amino group at the meta position and an acetic acid side chain. This unique arrangement contributes to its reactivity and versatility in chemical reactions. Searches for 2-(3-aminophenyl)acetic acid properties and solubility are common, as these parameters are crucial for its application in various processes.

One of the primary applications of 2-(3-aminophenyl)acetic acid is in the pharmaceutical industry, where it serves as a building block for drug development. Its amino and carboxylic acid groups allow for easy modification, making it ideal for creating derivatives with potential therapeutic effects. Recent trends show increased interest in pharmaceutical intermediates and drug synthesis, aligning with the compound's role in medicinal chemistry.

In addition to pharmaceuticals, 2-(3-aminophenyl)acetic acid finds use in agrochemicals and material science. Its ability to form stable complexes with metals makes it valuable in coordination chemistry and catalyst design. Researchers exploring green chemistry and sustainable synthesis often investigate this compound due to its potential in eco-friendly processes. The demand for biodegradable chemicals and non-toxic intermediates has further highlighted its relevance.

The synthesis of 2-(3-aminophenyl)acetic acid typically involves the reduction of corresponding nitro compounds or the hydrolysis of nitriles. Optimizing these methods for higher yields and purity is a frequent topic in organic synthesis forums and research publications. Users often search for 2-(3-aminophenyl)acetic acid synthesis steps and purification techniques, emphasizing the need for detailed procedural information.

From a commercial perspective, 2-(3-aminophenyl)acetic acid is available from specialized chemical suppliers. Quality parameters such as purity levels, packaging options, and bulk pricing are critical for buyers. The rise of online chemical marketplaces has made accessing this compound easier, with searches for CAS 14338-36-4 suppliers and 2-(3-aminophenyl)acetic acid price becoming more frequent.

Safety and handling of 2-(3-aminophenyl)acetic acid are also important considerations. While not classified as highly hazardous, proper storage conditions and material safety data sheets (MSDS) are essential for laboratory and industrial use. Queries related to chemical storage guidelines and handling precautions reflect user concerns about workplace safety.

In conclusion, 2-(3-aminophenyl)acetic acid (CAS No. 14338-36-4) is a multifaceted compound with broad applications in pharmaceuticals, agrochemicals, and material science. Its structural features and reactivity make it a valuable asset in synthetic chemistry. As interest in specialty chemicals and custom synthesis grows, this compound continues to attract attention from researchers and industries worldwide.

• 887589-14-2(1,2-Benzenediaceticacid, 4-amino-)
• 705240-99-9(2-(4-Amino-3-methylphenyl)acetic acid)
• 886363-12-8(3'-Amino-biphenyl-4-acetic Acid)
• 21762-11-8(2-(3-aminophenyl)propanoic acid)
• 54941-46-7(2-Amino-4-(carboxymethyl)toluene)
• 34841-55-9(1-(4-Amino-2-methylphenyl)acetic Acid)
• 621-43-2(2-(3,4-Diaminophenyl)acetic Acid)
• 75852-46-9([1,1'-Biphenyl]-3-aceticacid, 5-amino-)
• 1197-55-3(4-Aminophenylacetic acid)
• 886363-11-7([1,1'-Biphenyl]-3-aceticacid, 3'-amino-)