|  | |  |  | 2-Bromonaphthalene Basic information | 
|  |  | 2-Bromonaphthalene Chemical Properties | 
 | Melting point | 52-55 °C (lit.) |  | Boiling point | 281-282 °C (lit.) |  | density | 1,605 g/cm3 |  | refractive index | 1.6382 |  | Fp | >230 °F |  | storage temp. | Keep in dark place,Sealed in dry,Room Temperature |  | solubility | methanol: soluble50mg/mL, clear, colorless to yellow |  | form | Liquid |  | color | Clear light yellow to orange-brown |  | Water Solubility | slightly soluble |  | Merck | 14,1426 |  | BRN | 1858110 |  | InChIKey | APSMUYYLXZULMS-UHFFFAOYSA-N |  | CAS DataBase Reference | 580-13-2(CAS DataBase Reference) |  | NIST Chemistry Reference | 2-Bromonaphthalene(580-13-2) |  | EPA Substance Registry System | Naphthalene, 2-bromo- (580-13-2) | 
| Hazard Codes |  |  | RIDADR | UN1230 - class 3 - PG 2 - Methanol |  | WGK Germany | 3 |  | HS Code | 29039990 | 
|  |  | 2-Bromonaphthalene Usage And Synthesis | 
 | Chemical Properties | White or pale yellow powder |  | Uses | 2-Bromonaphthalene is used as a raw material in the preparation of biaryls through Suzuki cross coupling reaction. Further, it plays a vital role in the preparation of dyes. It is also used to study potential tumorigenicity. |  | Synthesis Reference(s) | The Journal of Organic Chemistry, 32, p. 1607, 1967 DOI: 10.1021/jo01280a069 Tetrahedron Letters, 26, p. 5939, 1985 DOI: 10.1016/S0040-4039(00)98266-2
 |  | General Description | Reaction of 2-bromonaphthalene with cuprous cyanide in N-methylpyrrolidone has been investigated. Nanosecond time-resolved resonance Raman spectra of the T1→Tn transition of 2-bromonaphthalene in methanol solvent has been investigated. |  | Purification Methods | Purify 2-bromonaphthalene by fractional elution from a chromatographic column of activated alumina. Crystallise it from EtOH. [Beilstein 5 IV 1667.] | 
|  |  | 2-Bromonaphthalene Preparation Products And Raw materials | 
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