Computed Properties of 19111-87-6, 2-Bromotriphenylene is a useful research compound. Its molecular formula is C18H11Br and its molecular weight is 307.2 g/mol. The purity is usually 95%.
2-Bromotriphenylene is a brominating agent that has the ability to react with sodium carbonate and emit light. The luminescence of 2-bromotriphenylene can be used as an indicator of the degree of dilution, or how much water is present in a solution. It also emits light when it reacts with chloride ions in a reaction solution. 2-Bromotriphenylene can be used as a polymer matrix to form polymeric films, which are then used as catalysts for organic reactions. The luminescence properties of 2-bromotriphenylene make it suitable for use in functional theory experiments. This chemical compound is relatively low cost, and has been shown to have high yield in catalysis., 19111-87-6.
A variety of minor organobromine compounds are found in nature, but none are biosynthesized or required by mammals. 19111-87-6, formula is C18H11Br, Name is 2-Bromotriphenylene. Organobromine compounds have fallen under increased scrutiny for their environmental impact., Computed Properties of 19111-87-6.
Barker, C. C.;Emmerson, R. G.;Periam, J. D. research published 《 Monosubstitution of triphenylene》, the research content is summarized as follows. The orientations of the products obtained by mononitration and by monobromination of triphenylene (I) were established, and the results discussed in the light of the predicted reactivity of I. 2-(1-Cyclohexen-1-yl)-1-(p-methoxyphenyl)cyclohexan-1-o1 (6 g.) and 4.6 g. monoperphthalic acid kept 16 hrs. at 0° in Et2O gave 6.3 g. liquid, this liquid refluxed 24 hrs. with 44 cc. 34% HBr and 63 cc. AcOH, solution diluted with H2O, and extracted with C6H6 gave 5.4 g. of residue. The residue heated 4 hrs. at 300° with Pd-C under N and the product sublimed at 200-20°/10-2 mm., the sublimate extracted with KOH solution, and acidified gave 2-hydroxytriphenylene (II), m. 215-17° (from PhCl). I gave Na triphenylene-2-sulfonate (III) in 70% yield and III was converted into 72% crude II. Sublimation and crystallization gave 27% II based on III; picrate, m. 224-5° (decomposition); Me ether, m. 119° (from light petroleum); acetyl derivative, m. 130°. Refluxing an aqueous suspension of triphenylene-2-diazonium chloride, followed by sublimation and crystallization gave II isolated as the picrate. I (5 g.) in 40 cc. PhNO2 containing 3.5 g. AlCl3 mixed at 0° with 1.75 cc. AcCl, left 20 hrs. at room temperature, and 4 hrs. at 40° gave 5.25 g. 2-acetyltriphenylene (IV), m. 152-3° (from EtOH). IV (10 g.) in dioxane oxidized 1 hr. at 60° with 24 g. Br in 180 cc. H2O containing 24 g. NaOH gave 8.3 g. triphenylene-2-carboxylic acid (V), m. 336-8° (from C5H11OH); Me ester, m. 171-2°; acid chloride (90% yield), m. 130-1°; amide (VI), m. 292-3° (from C5H5N); azide (VII), m. 135°. VII and PhCH2OH gave benzyl N-(2-triphenylenyl)carbamate, m. 169-70°, which failed to give 2-aminotriphenylene (VIII) when heated at 140° with AcOH and concentrated HCl. Nitric acid (70%, 167 cc.) added 45 min. to 6 g. I in Ac2O at 60°, the mixture kept at 60° for 4 hrs. and the product chromatographed on Al2O3 yielded 0.23 g. unchanged I, 1.96 g. 1-nitrotriphenylene (IX), m. 168.5-9.5°, and 1.63 g. 2-nitrotriphenylene, m. 165.5-6.0°. VII (3.5 g.), 100 cc. concentrated HCl, and 100 cc. AcOH refluxed 7 hrs. and the precipitate sublimed at 170-80°/10-2 mm. gave 1.74 g. VIII, m. 140.0-0.5° (from EtOH); N-acetyl derivative, m. 257-8°. VI (0.9 g.) in MeOH containing 0.4 g. NaOEt treated 15 min. at 50° with 0.3 g. Br gave 0.35 g. Me N-(2-triphenylenyl)-carbamate (X), m. 188-9°. X (0.4 g.) refluxed 24 hrs. with 20 cc. concentrated HCl and AcOH gave 0.07 g. VIII. HCl passed for 2.5 hrs. into a refluxing mixture of AcOH and concentrated HCl containing 3.5 g. granulated Sn and 1.96 g. IX yielded 0.94 g. 1-aminotriphenylene, m. 103-4° (from EtOH). VIII (0.25 g.) in AcOH poured into 20% HBr to precipitate the amine-HBr salt which was diazotized at 0° with NaNO2 in H2O, the diazonium salt refluxed 0.5 hr. with 1.2 g. CuBr in 6 cc. 40% HBr, and the product sublimed at 160-80°/10-2 mm. gave 0.1 g. 2-bromotriphenylene (XI), m. 131-2°. I (2 g.) in CCl4 containing 0.09 g. Fe powder treated 72 hrs. at 20° with 1.4 g. Br and the crude product chromatographed on Al2O3 gave 1.49 g. XI. No 1-bromotriphenylene could be isolated. If present at all, then it would have to be formed in much smaller amounts than XI.
Computed Properties of 19111-87-6, 2-Bromotriphenylene is a useful research compound. Its molecular formula is C18H11Br and its molecular weight is 307.2 g/mol. The purity is usually 95%.
2-Bromotriphenylene is a brominating agent that has the ability to react with sodium carbonate and emit light. The luminescence of 2-bromotriphenylene can be used as an indicator of the degree of dilution, or how much water is present in a solution. It also emits light when it reacts with chloride ions in a reaction solution. 2-Bromotriphenylene can be used as a polymer matrix to form polymeric films, which are then used as catalysts for organic reactions. The luminescence properties of 2-bromotriphenylene make it suitable for use in functional theory experiments. This chemical compound is relatively low cost, and has been shown to have high yield in catalysis., 19111-87-6.
Referemce:
Bromide – Wikipedia,
bromide – Wiktionary