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Hexafluoroethane | CAS:76-16-4
Hexafluoroethane
  • 名称:六氟乙烷 | Hexafluoroethane
  • CAS号:76-16-4
  • 别名:1,1,1,2,2,2-Hexafluoroethane; Ethyl hexafluoride; F 116; F 116 (fluorocarbon); FC 116; FC 1160; Freon 116; HFC 116; Hexafluoroethane; PFC 116; Perfluorocarbon 116; Perfluoroethane; R 116
  • 分子式:C2F6
  • 分子量:138.01
  • EINESC号:200-939-8

产品描述

物理化学性质

熔点 106.3 ºC**
沸点 -19 ºC***
闪点 -60.9±10.4 ºC, 计算值****
密度 1.85 g/cm3 (-192 ºC)*

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来源 SDS样本
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The synthesis and evaluation of quinolinequinones as anti-mycobacterial agents.Kristiana T Santoso et al.Bioorganic & medicinal chemistry, 27(16), 3532-3545 (2019-07-03) New type of arrangement of rare-earth quinolinolate. Molecular structure of scandium 2-methyl-8-quinolinolate.Katkova MA, et al. Inorgorganica Chimica Acta, 362(4), 1393-1395 (2009) Synthesis, Electrochemical and Spectroscopic Characterization of Selected Quinolinecarbaldehydes and Their Schiff Base Derivatives.Jakub Wantulok et al.Molecules (Basel, Switzerland), 25(9) (2020-05-02) Exploring molecular shape analysis of styrylquinoline derivatives as HIV-1 integrase inhibitors.J Thomas Leonard et al.European journal of medicinal chemistry, 43(1), 81-92 (2007-04-25) The crystal and molecular structure of bis-(2-methyl-8-quinolinolato) oxovanadium (IV).Shiro M and Fernando Q. Journal of the Chemical Society. Chemical Communications, 1, 63-64 (1971) Studies on antitumor mechanism of two planar platinum(II) complexes with 8-hydroxyquinoline: synthesis, characterization, cytotoxicity, cell cycle and apoptosis.Qi-Pin Qin et al.European journal of medicinal chemistry, 92, 302-313 (2015-01-13) Infrared Spectra, Density Functional Theory and Hartree-Fock Theoretical Calculations of 2-Methyl-8-quinolinol.Arici K and Yilmaz R. Asian Journal of Chemistry, 25(13), 7106-7106 (2013) Design and synthesis of conjugated azo-hydrazone analogues using nano BFZabiulla et al.Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie, 95, 419-428 (2017-09-02) Antifungal activity of 5-,7-, and 5,7-substituted 2-methyl-8-quinolinols.Gershon H, et al. Antimicrobial Agents and Chemotherapy, 1(5), 373-375 (1972) Identifying chelators for metalloprotein inhibitors using a fragment-based approach.Jennifer A Jacobsen et al.Journal of medicinal chemistry, 54(2), 591-602 (2010-12-30)
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