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| | 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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