≥99% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Room temperature Ships Normal Check lot-specific COA for exact specifications.
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.
2,6-Dibromonaphthalene is an important raw material and intermediate used in organic synthesis, pharmaceuticals and agrochemicals. It reacts with hexylmagnesium bromide to form 2,6-Dihexyl-naphthalene.
| Pubchem Sid | 508807809 |
|---|---|
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/508807809 |
| Sorrisos canónicos | C1=CC2=C(C=CC(=C2)Br)C=C1Br |
| IUPAC Name | 2,6-dibromonaphthalene |
| InChIKey | PJZDEYKZSZWFPX-UHFFFAOYSA-N |
| INCHI | 1S/C10H6Br2/c11-9-3-1-7-5-10(12)4-2-8(7)6-9/h1-6H |
| SMILES isoméricas | C1=CC2=C(C=CC(=C2)Br)C=C1Br |
| WGK Alemanha | 3 |
| Peso molecular | 285.96 |
| Reaxy-Rn | 1935714 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1935714&ln= |
Comprehensive hazard, handling, storage, and regulatory compliance document.
Download SDS →Lot-specific quality data. Enter your lot number to retrieve the exact COA.
Look up COA →Full quality attributes and acceptance criteria for this grade.
View spec sheet →Taxonomy Tree
| Kingdom | Organic compounds |
|---|---|
| Superclass | Benzenoids |
| Classe | Naphthalenes |
| Subclass | Not available |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Naphthalenes |
| Alternative Parents | Aryl bromides Organobromides Hydrocarbon derivatives |
| Molecular Framework | Aromatic homopolycyclic compounds |
| Substituents | Naphthalene - Aryl halide - Aryl bromide - Hydrocarbon derivative - Organobromide - Organohalogen compound - Aromatic homopolycyclic compound |
| Descrição | This compound belongs to the class of organic compounds known as naphthalenes. These are compounds containing a naphthalene moiety, which consists of two fused benzene rings. |
| External Descriptors | Not available |
Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Data | Item |
|---|---|---|---|
 L2121343 | Certificate of Analysis | Jun 09, 2025 | D101017 |
| L2121344 | Certificate of Analysis | Jun 09, 2025 | D101017 |
| L2121418 | Certificate of Analysis | Jun 09, 2025 | D101017 |
| F2314227 | Certificate of Analysis | Mar 05, 2025 | D101017 |
| A2105174 | Certificate of Analysis | Jul 11, 2024 | D101017 |
| F1502002 | Certificate of Analysis | Jul 11, 2024 | D101017 |
| Solubilidade | Insoluble in water. |
|---|---|
| Ponto de fusão (°C) | 162-167°C |
| Peso molecular | 285.960 g/mol |
| XLogP3 | 4.600 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 0 |
| Rotatable Bond Count | 0 |
| Exact Mass | 285.882 Da |
| Monoisotopic Mass | 283.884 Da |
| Topological Polar Surface Area | 0.000 Ų |
| Heavy Atom Count | 12 |
| Formal Charge | 0 |
| Complexity | 140.000 |
| 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 |
