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9,10-二氢菲

9,10-二氢菲是一种有机化合物,化学式为C14H12。它可由在催化下加氢制得[2]。它可以被混酸[3]硝酸铋[4]硝化,得到2,7-二硝基-9,10-二氢菲;它在三氯化铁催化下和反应,可以得到2,7-二溴-9,10-二氢菲[5]

9,10-二氢菲
识别
CAS号 776-35-2  Y
SMILES
 
  • C=1C=CC2=C(C1)C=3C=CC=CC3CC2
性质
化学式 C14H12
摩尔质量 180.25 g·mol−1
熔点 35-35.5 °C(308.1-308.6 K)[1]
若非注明,所有数据均出自标准状态(25 ℃,100 kPa)下。

参考文献 编辑

  1. ^ Hall, D. Muriel; Lesslie, Mary S.; Turner, E. E. 143. 9 : 10-Dihydrophenanthrenes. Part I. The formation of 9 : 10-dihydrophenanthrene from 2 : 2′-disubstituted diphenyls. J. Chem. Soc. (Royal Society of Chemistry (RSC)). 1950, 0 (0): 711–713. ISSN 0368-1769. doi:10.1039/jr9500000711. 
  2. ^ Amer, Ibrahim; Amer, Hamdullah; Ascher, Rachel; Blum, Jochanan; Sasson, Yoel; Vollhardt, K.Peter C. Hydrogenation of arenes by the RhCl3-aliquat® 336 catalyst. Journal of Molecular Catalysis. 1987-02, 39 (2): 185–194. doi:10.1016/0304-5102(87)80062-7. 
  3. ^ Nelsen, Stephen F.; Luo, Yun; Weaver, Michael N.; Lockard, Jenny V.; Zink, Jeffrey I. Optical Spectra of Protected Diamine 10-Bond-Bridged Intervalence Radical Cations Related to N,N,NN‘-Tetraalkylbenzidine. The Journal of Organic Chemistry (American Chemical Society (ACS)). 2006-05-01, 71 (11): 4286–4295. ISSN 0022-3263. doi:10.1021/jo060466l. 
  4. ^ Yadav, Ram N.; Salazar, Leonardo; Singh, Amrendra Kumar; Banik, Bimal Krishna. Microwave-induced bismuth nitrate-impregnated clay-mediated novel dinitration of 9,10- dihydrophenanthrene: a precursor for new heterocycles. Heterocyclic Letters, 2018. 8 (2): 273-276.
  5. ^ Sasaki, Shunsuke; Niko, Yosuke; Klymchenko, Andrey S.; Konishi, Gen-ichi. Design of donor–acceptor geometry for tuning excited-state polarization: fluorescence solvatochromism of push–pull biphenyls with various torsional restrictions on their aryl–aryl bonds. Tetrahedron (Elsevier BV). 2014, 70 (41): 7551–7559. ISSN 0040-4020. doi:10.1016/j.tet.2014.08.002. 

二氢菲, 是一种有机化合物, 化学式为c14h12, 它可由菲在催化下加氢制得, 它可以被混酸, 或硝酸铋, 硝化, 得到2, 二硝基, 它在三氯化铁催化下和溴反应, 可以得到2, 二溴, 识别cas号, ysmiles, cc3cc2性质化学式, c14h12摩尔质量, 1熔点, 若非注明, 所有数据均出自标准状态, 参考文献, 编辑, hall, muriel, lesslie, mary, turner, dihydrophenanthrenes, part, formation, dihydrophenan. 9 10 二氢菲是一种有机化合物 化学式为C14H12 它可由菲在催化下加氢制得 2 它可以被混酸 3 或硝酸铋 4 硝化 得到2 7 二硝基 9 10 二氢菲 它在三氯化铁催化下和溴反应 可以得到2 7 二溴 9 10 二氢菲 5 9 10 二氢菲识别CAS号 776 35 2 YSMILES C 1C CC2 C C1 C 3C CC CC3CC2性质化学式 C14H12摩尔质量 180 25 g mol 1熔点 35 35 5 C 308 1 308 6 K 1 若非注明 所有数据均出自标准状态 25 100 kPa 下 参考文献 编辑 Hall D Muriel Lesslie Mary S Turner E E 143 9 10 Dihydrophenanthrenes Part I The formation of 9 10 dihydrophenanthrene from 2 2 disubstituted diphenyls J Chem Soc Royal Society of Chemistry RSC 1950 0 0 711 713 ISSN 0368 1769 doi 10 1039 jr9500000711 Amer Ibrahim Amer Hamdullah Ascher Rachel Blum Jochanan Sasson Yoel Vollhardt K Peter C Hydrogenation of arenes by the RhCl3 aliquat 336 catalyst Journal of Molecular Catalysis 1987 02 39 2 185 194 doi 10 1016 0304 5102 87 80062 7 Nelsen Stephen F Luo Yun Weaver Michael N Lockard Jenny V Zink Jeffrey I Optical Spectra of Protected Diamine 10 Bond Bridged Intervalence Radical Cations Related to N N N N Tetraalkylbenzidine The Journal of Organic Chemistry American Chemical Society ACS 2006 05 01 71 11 4286 4295 ISSN 0022 3263 doi 10 1021 jo060466l Yadav Ram N Salazar Leonardo Singh Amrendra Kumar Banik Bimal Krishna Microwave induced bismuth nitrate impregnated clay mediated novel dinitration of 9 10 dihydrophenanthrene a precursor for new heterocycles Heterocyclic Letters 2018 8 2 273 276 Sasaki Shunsuke Niko Yosuke Klymchenko Andrey S Konishi Gen ichi Design of donor acceptor geometry for tuning excited state polarization fluorescence solvatochromism of push pull biphenyls with various torsional restrictions on their aryl aryl bonds Tetrahedron Elsevier BV 2014 70 41 7551 7559 ISSN 0040 4020 doi 10 1016 j tet 2014 08 002 取自 https zh wikipedia org w index php title 9 10 二氢菲 amp oldid 79721296, 维基百科,wiki,书籍,书籍,图书馆,

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