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• Solvents and Organic Chemicals Organic Compounds Organoheterocyclic compounds Indoles and derivatives Carbazoles

Comprehensive Overview of 2-(9H-Carbazol-3-yl)acetic acid (CAS No. 374916-11-7): Properties, Applications, and Industry Trends

2-(9H-Carbazol-3-yl)acetic acid (CAS No. 374916-11-7) is a specialized organic compound gaining attention in pharmaceutical and material science research. This carbazole derivative features a unique molecular structure combining a carbazole core with an acetic acid functional group, making it valuable for diverse applications. Researchers increasingly focus on this compound due to its potential in OLED materials, drug intermediates, and bioconjugation chemistry.

The compound's molecular formula C14H11NO2 and molecular weight 225.24 g/mol position it as a versatile building block. Recent studies highlight its role in developing fluorescent probes for biological imaging, aligning with the growing demand for bioimaging agents in medical diagnostics. The carbazole moiety contributes to its electron-transport properties, particularly relevant for organic electronic devices – a hot topic in sustainable technology discussions.

From a synthetic chemistry perspective, 2-(9H-Carbazol-3-yl)acetic acid serves as a crucial intermediate for creating more complex heterocyclic compounds. Its carboxylic acid group enables various derivatization reactions, including esterification and amide formation, answering frequent search queries about carbazole functionalization methods. The compound's solubility profile (soluble in polar organic solvents but insoluble in water) makes it particularly useful for solution-processed materials – a key phrase in materials science forums.

Quality specifications for CAS 374916-11-7 typically require ≥95% purity by HPLC, with analytical methods including 1H NMR and mass spectrometry verification. Storage recommendations suggest keeping the compound at 2-8°C under inert atmosphere, addressing common questions about carbazole compound stability. The material's melting point range (typically 200-205°C) and UV-Vis absorption characteristics (λmax ~290 nm) are frequently cited in technical datasheets.

Emerging applications leverage the compound's photophysical properties for solar cell materials, connecting to renewable energy trends. The carbazole-acetic acid conjugate structure shows promise in small molecule drug development, particularly for targeting protein-protein interactions – a trending topic in medicinal chemistry. Recent patent literature reveals growing interest in using this scaffold for kinase inhibitor design.

Safety data indicates 2-(9H-Carbazol-3-yl)acetic acid requires standard laboratory precautions, with no extreme hazards reported. This safety profile makes it attractive for academic research and industrial scale-up – two frequently searched terms by chemistry professionals. The compound's structure-activity relationships continue to be explored, particularly how modifications affect its electronic properties and biological activity.

Market analysis shows increasing demand for high-purity carbazole derivatives, driven by advancements in organic electronics and pharmaceutical research. Suppliers typically offer CAS 374916-11-7 in gram to kilogram quantities, with custom synthesis options available. Pricing trends reflect the compound's specialized nature and the complexity of its multi-step synthesis from carbazole precursors.

Future research directions may explore the compound's potential in metal-organic frameworks (MOFs) and covalent organic frameworks (COFs) – currently trending topics in materials science. Its dual functionality (carbazole for π-stacking and carboxylic acid for coordination) makes it particularly interesting for designing porous materials with tailored properties. These applications answer growing search queries about advanced functional materials.

In conclusion, 2-(9H-Carbazol-3-yl)acetic acid represents an important chemical building block with expanding applications across multiple disciplines. Its combination of aromatic character and acid functionality provides unique opportunities for molecular design, addressing current research needs in materials science, medicinal chemistry, and molecular engineering. The compound's versatility ensures its continued relevance in cutting-edge scientific developments.

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• 886363-20-8(3-(5'-Indole)Phenyl Acetic Acid)
• 51035-18-8(9H-Carbazole-2-acetic acid)
• 152149-07-0(2-(quinolin-7-yl)acetic acid)
• 39689-58-2(2-(1H-Indol-6-yl)acetic acid)
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• 109922-57-8(2-(Quinolin-4-yl)acetic acid)
• 76937-78-5(3-Indoleacetic acid-d)