≥98% 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.
Product Description
Two-photon chemistry of 1,8-bis(bromomethyl)naphthalene has been studied by time-delayed, two-color photolysis and argon ion laser-jet photolysis techniques.
Product Application
1,8-Bis(bromomethyl)naphthalene has been used in the synthesis of indan-based unusual α-amino acid derivatives under solid-liquid phase-transfer catalysis conditions.
| Pubchem Sid | 488189314 |
|---|---|
| Sonrisas canónicas | C1=CC2=C(C(=C1)CBr)C(=CC=C2)CBr |
| IUPAC Name | 1,8-bis(bromomethyl)naphthalene |
| InChIKey | GCZOMCDXYFMAGP-UHFFFAOYSA-N |
| INCHI | 1S/C12H10Br2/c13-7-10-5-1-3-9-4-2-6-11(8-14)12(9)10/h1-6H,7-8H2 |
| Isómeros SMILES | C1=CC2=C(C(=C1)CBr)C(=CC=C2)CBr |
| WGK Alemania | 3 |
| Número ONU | 3261 |
| Grupo de embalaje | II |
| Peso molecular | 314.02 |
| Reaxy-Rn | 1951395 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1951395&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 |
| Clase | Naphthalenes |
| Subclass | Not available |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Naphthalenes |
| Alternative Parents | Organobromides Hydrocarbon derivatives Alkyl bromides |
| Molecular Framework | Aromatic homopolycyclic compounds |
| Substituents | Naphthalene - Hydrocarbon derivative - Organobromide - Organohalogen compound - Alkyl halide - Alkyl bromide - Aromatic homopolycyclic compound |
| Descripción | 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 | Fecha | Articulo |
|---|---|---|---|
 D2304476 | Certificate of Analysis | Apr 17, 2023 | B359056 |
| D2304446 | Certificate of Analysis | Apr 15, 2023 | B359056 |
| D2304448 | Certificate of Analysis | Apr 15, 2023 | B359056 |
| D2304474 | Certificate of Analysis | Apr 15, 2023 | B359056 |
| F23021084 | Certificate of Analysis | Apr 15, 2023 | B359056 |
| Punto de fusión (°C) | 131 - 133 °C |
|---|---|
| Peso molecular | 314.010 g/mol |
| XLogP3 | 4.300 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 0 |
| Rotatable Bond Count | 2 |
| Exact Mass | 313.913 Da |
| Monoisotopic Mass | 311.915 Da |
| Topological Polar Surface Area | 0.000 Ų |
| Heavy Atom Count | 14 |
| Formal Charge | 0 |
| Complexity | 163.000 |
| 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 |
