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SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Methyl 6-bromo-2-naphthoate undergoes aromatic Finkelstein reaction followed by hydrolysis to afford 6-iodo-2-naphthoic acid.
| Pubchem Sid | 488191648 |
|---|---|
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/488191648 |
| Canonical Smiles | COC(=O)C1=CC2=C(C=C1)C=C(C=C2)Br |
| IUPAC Name | methyl 6-bromonaphthalene-2-carboxylate |
| InChIKey | JEUBRLPXJZOGPX-UHFFFAOYSA-N |
| INCHI | 1S/C12H9BrO2/c1-15-12(14)10-3-2-9-7-11(13)5-4-8(9)6-10/h2-7H,1H3 |
| Isomeric SMILES | COC(=O)C1=CC2=C(C=C1)C=C(C=C2)Br |
| WGK Germany | 3 |
| Molecular Weight | 265.11 |
| Reaxy-Rn | 2578943 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2578943&ln= |
Comprehensive hazard, handling, storage, and regulatory compliance document.
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View spec sheet →Taxonomy Tree
| Kingdom | Organic compounds |
|---|---|
| Superclass | Benzenoids |
| Class | Naphthalenes |
| Subclass | Naphthalenecarboxylic acids and derivatives |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Naphthalenecarboxylic acids |
| Alternative Parents | Aryl bromides Methyl esters Monocarboxylic acids and derivatives Organooxygen compounds Organobromides Organic oxides Hydrocarbon derivatives |
| Molecular Framework | Aromatic homopolycyclic compounds |
| Substituents | 2-naphthalenecarboxylic acid - Aryl halide - Aryl bromide - Methyl ester - Carboxylic acid ester - Monocarboxylic acid or derivatives - Carboxylic acid derivative - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Organobromide - Organohalogen compound - Aromatic homopolycyclic compound |
| Description | This compound belongs to the class of organic compounds known as naphthalenecarboxylic acids. These are compounds containing a naphthalene moiety, which bears a carboxylic acid group one or more positions. Naphthalene is a bicyclic compound that is made up of two fused benzene ring. |
| External Descriptors | Not available |
Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Date | Item |
|---|---|---|---|
| Certificate of Analysis | Feb 05, 2026 | M135084 | |
| Certificate of Analysis | Feb 05, 2026 | M135084 | |
| Certificate of Analysis | Jan 26, 2026 | M135084 | |
| Certificate of Analysis | Oct 21, 2025 | M135084 | |
| Certificate of Analysis | Dec 17, 2024 | M135084 | |
| Certificate of Analysis | Dec 17, 2024 | M135084 | |
| Certificate of Analysis | Dec 17, 2024 | M135084 | |
| Certificate of Analysis | Dec 17, 2024 | M135084 | |
| Certificate of Analysis | Dec 06, 2024 | M135084 | |
| Certificate of Analysis | Dec 06, 2024 | M135084 | |
| Certificate of Analysis | Dec 06, 2024 | M135084 | |
| Certificate of Analysis | Dec 30, 2022 | M135084 |
| Melt Point(°C) | 118 - 126°C |
|---|---|
| Molecular Weight | 265.100 g/mol |
| XLogP3 | 3.700 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 2 |
| Rotatable Bond Count | 2 |
| Exact Mass | 263.979 Da |
| Monoisotopic Mass | 263.979 Da |
| Topological Polar Surface Area | 26.300 Ų |
| Heavy Atom Count | 15 |
| Formal Charge | 0 |
| Complexity | 242.000 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| The total count of all stereochemical bonds | 0 |
| Covalently-Bonded Unit Count | 1 |