Cas no 136415-64-0 (2-Naphthalenecarboxylic acid, 8-(bromomethyl)-, methyl ester)

2-Naphthalenecarboxylic acid, 8-(bromomethyl)-, methyl ester is a brominated naphthalene derivative with significant utility in organic synthesis. The compound features a reactive bromomethyl group at the 8-position, enabling efficient functionalization through nucleophilic substitution or cross-coupling reactions. Its ester group enhances solubility in organic solvents, facilitating handling in synthetic applications. This intermediate is particularly valuable in pharmaceutical and materials chemistry for constructing complex naphthalene-based scaffolds. The bromomethyl moiety offers precise control over further derivatization, making it a versatile building block for targeted molecular design. High purity and consistent reactivity ensure reliable performance in demanding synthetic workflows.
2-Naphthalenecarboxylic acid, 8-(bromomethyl)-, methyl ester structure
136415-64-0 structure
Product Name:2-Naphthalenecarboxylic acid, 8-(bromomethyl)-, methyl ester
CAS No:136415-64-0
MF:C13H11BrO2
MW:279.129243135452
CID:1246127
Update Time:2025-10-23

2-Naphthalenecarboxylic acid, 8-(bromomethyl)-, methyl ester Chemical and Physical Properties

Names and Identifiers

    • 2-Naphthalenecarboxylic acid, 8-(bromomethyl)-, methyl ester
    • methyl 8-bromomethyl-2-naphthoate
    • Methyl 1-(bromomethyl)naphthalene-7-carboxylate
    • Inchi： 1S/C13H11BrO2/c1-16-13(15)10-6-5-9-3-2-4-11(8-14)12(9)7-10/h2-7H,8H2,1H3
    • InChI Key： OKVKCRRYNXCTOQ-UHFFFAOYSA-N
    • SMILES： C1=C2C(C=CC=C2CBr)=CC=C1C(OC)=O

Computed Properties

  • Exact Mass: 277.99423

Experimental Properties

  • Density: 1.461±0.06 g/cm3(Predicted)
  • Boiling Point: 380.6±17.0 °C(Predicted)
  • PSA: 26.3

2-Naphthalenecarboxylic acid, 8-(bromomethyl)-, methyl ester Pricemore >>

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2-Naphthalenecarboxylic acid, 8-(bromomethyl)-, methyl ester Related Literature

Additional information on 2-Naphthalenecarboxylic acid, 8-(bromomethyl)-, methyl ester

Comprehensive Overview of 2-Naphthalenecarboxylic acid, 8-(bromomethyl)-, methyl ester (CAS No. 136415-64-0)

2-Naphthalenecarboxylic acid, 8-(bromomethyl)-, methyl ester (CAS No. 136415-64-0) is a specialized organic compound widely utilized in pharmaceutical intermediates, agrochemical synthesis, and advanced material research. Its unique structure, featuring a naphthalene backbone with a bromomethyl substituent and a methyl ester group, makes it a versatile building block for diverse chemical transformations. Researchers and industries value this compound for its role in coupling reactions, polymer modifications, and as a precursor for bioactive molecules.

In recent years, the demand for 2-Naphthalenecarboxylic acid derivatives has surged due to their applications in OLED materials and organic electronics. The bromomethyl functional group enables facile further functionalization, aligning with the growing trend of modular synthesis in green chemistry. Environmental concerns and regulatory shifts have also driven interest in halogenated intermediates like this compound, as they balance reactivity with manageable ecological footprints.

Analytical techniques such as HPLC, NMR, and mass spectrometry are critical for characterizing CAS No. 136415-64-0. Purity standards often exceed 98% for research-grade batches, ensuring reproducibility in cross-coupling reactions. The compound’s stability under inert atmospheres and sensitivity to moisture are frequently discussed in technical forums, reflecting user priorities for storage protocols.

Emerging studies explore its potential in photoredox catalysis—a hot topic in synthetic chemistry. The naphthalene core’s conjugated system enhances light absorption properties, making it relevant for sustainable energy solutions. This aligns with frequent search queries like "naphthalene derivatives in catalysis" or "bromomethyl applications in organic synthesis", highlighting its interdisciplinary relevance.

Supply chain dynamics for 8-(bromomethyl)-2-naphthoate (an alternative name) reflect broader market trends. With Asia-Pacific manufacturers scaling production, cost-effectiveness has improved, though quality verification remains essential. Regulatory compliance, particularly regarding halogenated compounds, is another key search focus, emphasizing the need for transparent SDS documentation.

Future directions may involve derivatization for biodegradable polymers or non-toxic flame retardants—addressing sustainability demands. Patent analyses reveal growing IP activity around modified naphthalene esters, suggesting expanding industrial applications. For researchers, optimizing solvent systems for reactions involving this compound remains a practical challenge, often explored in academic literature.

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