CAS: 19430-93-4; 3,3,4,4,5,5,6,6,6-Nonafluorohex-1-Ene

该化合物是一种全氟化合物,其特点是存在与六氟骨柱相连的多种氟原子;该化合物具有六碳原子和双联结的碳链,其性质有助于其不饱和性;广泛的氟化具有独特的特性,如高热稳定性和化学稳定性,低表面张力和抗降解性,使其在各种应用中有用,包括特殊涂层和表面活性剂;其非极性特征和低再活性是全氟化合物的典型特征,这些化合物往往表现出水分恐惧行为;此外,双重联结的存在可影响其在某些化学过程中的再活动,尽管氟化环境一般限制这种再活动;由于其独特性,3,4,4,4,5,5,5,6,6,6-非氟己烷在工业应用和研究中,特别是在材料科学和环境化学领域,都对其有用.然而,围绕全氟化合物产生的环境影响和监管因素是其使用中需要考虑的重要因素.

结构式图片

欧盟法规

REACH注册ECHA物质ECHA物质C&L通报REACH预注册

上下游产品

CAS号1374104-94-5 1,3-bis(1-iodo-... | CAS号1374104-99-0 fluorodimethyl(... | CAS号2043-57-4 1,1,1,2,2,3,3,4... | CAS号10192-85-5 丙烯酸钾 | CAS号2043-55-2 全氟丁基乙基碘 | CAS号105-53-3 丙二酸二乙酯 | CAS号38436-14-5 6-溴-1,1,1,2,2,3... | CAS号38436-16-7 甲基(3,3,4,4,5,5,... | CAS号89807-87-4 1H,1H,2H-正氟-1,2-环氧己烷 | CAS号2043-47-2 全氟丁基乙醇 | CAS号116741-81-2 3,3,4,4,5,5,6,6... | CAS号154194-61-3 methyl(3,3,4,4,... | CAS号375-53-1 全氟pentanal 水合物 | CAS号78560-47-1 1H,1H,2H,2H-全氟己基三氯硅烷 | CAS号89807-81-8 acetic acid,2-b... | CAS号89807-84-1 2-bromo-3,3,4,4... | CAS号59665-30-4 3,3,4,4,5,5,6,6...

合成工艺路线路线简述

  • 合成目标产物 (Perfluorobutyl)Ethylene 主要起始原料 Disiloxane, 1,1,3,3-Tetramethyl-1,3-Bis(3,3,4,4,5,5,6,6,6-Nonafluoro-1-Iodohexyl)-
  • (文献来源)合成步骤主要原料 Disiloxane, 1,1,3,3-Tetramethyl-1,3-Bis(3,3,4,4,5,5,6,6,6-Nonafluoro-1-Iodohexyl)-
1,1,2,2-四氢全氟己基碘置于氢氧化钾体系中,用 乙醇 用作溶剂,化学反应生成1H,1H,2H-全氟-1-己烯
参考文献:Demarcq,M.; Sleziona,J.,Phosphorus And The Related Group V Elements,1974,Vol. 4,P. 173-178
标题:Demarcq,M.; Sleziona,J.,Phosphorus And The Related Group V Elements,1974,Vol. 4,P. 173-178

海关参考信息

专利信息


专利号:US-6794534-B2
优先权日:2000-06-23
标题:Synthesis of functionalized and unfunctionalized olefins via cross and ring-closing metathesis
发明人:GRUBBS ROBERT H; CHATTERJEE ARNAB K; MORGAN JOHN P; SCHOLL MATTHIAS; CHOI TAE-LIM
权利人:CALIFORNIA INST OF TECHN
摘要:The invention is directed to the cross-metathesis and ring-closing metathesis reactions between geminal disubstituted olefins and terminal olefins, wherein the reaction employs a Ruthenium or Osmium metal carbene complex. Specifically, the invention relates to the synthesis of α-functionalized or unfunctionalized olefins via intermolecular cross-metathesis and intramolecular ring-closing metathesis using a ruthenium alkylidene complex. The catalysts preferably used in the invention are of the general formula n wherein: n M is ruthenium or osmium; n X and X 1 are each independently an anionic ligand; n L is a neutral electron donor ligand; and, n R, R 1 R 6 , R 7 , R 8 , and R 9 are each independently hydrogen or a substituent selected from the group consisting of C 1 -C 20 alkyl, C 2 -C 20 alkenyl, C 2 -C 20 alkynyl, aryl, C 1 -C 20 carboxylate, C 1 -C 20 alkoxy, C 2 -C 20 alkenyloxy, C 2 -C 20 alkynyloxy, aryloxy, C 2 -C 20 alkoxycarbonyl, C 1 -C 20 alkylthio, C 1 -C 20 alkylsulfonyl and C 1 -C 20 alkylsulfinyl.

专利号:US-9394394-B2
优先权日:2013-09-30
标题:Synthesis of chlorotrifluoroethylene-based block copolymers by iodine transfer polymerization
发明人:THENAPPAN ALAGAPPAN; AMEDURI BRUNO; LOPEZ GERALD
权利人:HONEYWELL INT INC
摘要:Methods for the synthesis of CTFE-based block copolymers through iodine transfer polymerization are disclosed. In an exemplary embodiment, a method includes reacting a fluoromonomer “Mâ€? with a chain transfer agent of the formula X—Y or Y—X—Y, wherein X represents a C 1 -C 3 hydrocarbon, a C 1 -C 6 hydrofluorocarbon, C 1 -C 6 hydrochlorofluorocarbon, or C 1 -C 6 fluorocarbon and Y represents iodine or bromine, in the presence of a radical initiator, to form a macro-initiator of the formula: X-poly(M)-Y or Y-poly(M)-X-poly(M)-Y, wherein poly(M) represents a polymer of the fluoromonomer. The method further includes reacting the macro-initiator with chlorotrifluoroethylene (CTFE) in the presence of a radical initiator to form a diblock or a triblock CTFE-based block copolymer of the formula: X-poly(M)-block-poly(CTFE) or PCTFE-block-poly(M)-X-poly(M)-block-PCTFE.

专利号:US-9403854-B2
优先权日:2001-03-30
标 题 :Cross-metathesis reaction of functionalized and substituted olefins using group 8 transition metal carbene complexes as metathesis catalysts
发明人:GRUBBS ROBERT H; CHATTERJEE ARNAB K; CHOI TAE-LIM; GOLDBERG STEVEN D; LOVE JENNIFER A; MORGAN JOHN P; SANDERS DANIEL P; SCHOLL MATTHIAS; TOSTE F DEAN; TRNKA TINA M
权利人:CALIFORNIA INST OF TECHN
摘要:The invention pertains to the use of Group 8 transition metal carbene complexes as catalysts for olefin cross-metathesis reactions. In particular, ruthenium and osmium alkylidene complexes substituted with an N-heterocyclic carbene ligand are used to catalyze cross-metathesis reactions to provide a variety of substituted and functionalized olefins, including phosphonate-substituted olefins, directly halogenated olefins, 1,1,2-trisubstituted olefins, and quaternary allylic olefins. The invention further provides a method for creating functional diversity using the aforementioned complexes to catalyze cross-metathesis reactions of a first olefinic reactant, which may or may not be substituted with a functional group, with each of a plurality of different olefinic reactants, which may or may not be substituted with functional groups, to give a plurality of structurally distinct olefinic products. The methodology of the invention is also useful in facilitating the stereoselective synthesis of 1,2-disubstituted olefins in the cis configuration.

专利号:US-9284336-B1
优先权日:2014-08-21
标题 :Synthesis of 4-(pentafluorosulfanyl)benzenediazonium tetrafluoroborate and analogs
发明人:LAALI KENNETH K
权利人:LAALI KENNETH K; UNIV NORTH FLORIDA
摘要:4-(pentafluorosulfanyl)benzenediazonium tetrafluoroborate salt was synthesized and isolated. The pentafluorosulfanyl salt was examined in a wide assortment of reactions to form novel SF 5 -bearing alkenes, alkynes, and biaryl derivatives using Heck-Matsuda, Sonogashira, and Suzuki coupling protocols. Dediazoniation of the salt furnished the corresponding p-SF 5 —C 6 H 4 X, C 6 H 4 OS(O)(CF 3 )â•?NSO 2 CF 3 , and p-SF 5 —C 6 H 4 —NTf 2 derivatives. The azide derivative p-SF 5 —C 6 H 4 N 3 entered into click chemistry with phenylacetylenes to furnish the corresponding triazoles. Various SF 5 -bearing alkenes were synthesized by coupling reactions using a metal catalyst. Fluorodediazoniation selectively furnished the fluoro derivative p-SF 5 —C 6 H 4 F. Homolytic dediazoniation gave the unsymmetrical biaryls, thus demonstrating the broad utility of pentafluorosulfanyl diazonium salts as building blocks of SF5-aromatics that are in high demand in many branches of chemistry including biomedicine and materials chemistry.

专利号:US-5084583-A
优先权日:1989-10-12
标题:Epoxidation of fluorine containing olefins
发明人:ROZEN SHLOMO M; SMART BRUCE E
权利人:DU PONT
摘要:The synthesis of epoxides from fluorine containing olefins using elemental fluorine in mixtures of water and acetonitrile is disclosed.

专利号:EP-0495823-B1
优先权日:1989-10-12
标题 :Epoxidation of fluorine containing olefins
发明人:ROZEN SHLOMO M; SMART BRUCE EDMUND
权利人:DU PONT
摘要:The synthesis of epoxides from fluorine containing olefins using elemental fluorine in mixtures of water and acetonitrile is disclosed.
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✅ COA系统入驻 | 共享模式

主要参考文献

参考标题:Nickel-Catalyzed Allylic C(Sp3)-F Bond Activation Of Trifluoromethyl Groups Via β-Fluorine Elimination: Synthesis Of Difluoro-1,4-Dienes
作者:Tomohiro Ichitsuka,Takeshi Fujita,Junji Ichikawa |发布日期:2015.10.2
摘要:2-Trifluoromethyl-1-Alkenes And Alkynes With The Aid Of Et3Sih Provides 1,1-Difluoro-1,4-Dienes Under Mild Reaction Conditions. This Reaction Involves Selective Allylic C(Sp3)-F Bond Activation Via β-Fluorine Elimination From Nickelacyclopentenes.

合成参考文献


摘要:Michalak, M.; Gulajski, L.; Grela, K., Science of Synthesis, (2010) 47, 354.
摘要:Liang, Y.; Wen, Z.; Cabrera, M.; Howlader, A. H.; Wnuk, S. F., Science of Synthesis Knowledge Updates, (2020) 1, 243.
摘要:CRC Critical Reviews in Toxicology., 21(149), 1990 []
摘要:Lyman WJ et al; Handbook of Chemical Property Estimation Methods. Washington, DC: Amer Chem Soc pp. 7-4, 7-5, 8-12 (1990)
摘要:Sigma-Aldrich; Material Safety Data Sheet for 1H,1H,2H-Perfluoro-1-hexene. Product Number 371459. Version 4.0, Revision Date July 25, 2010. Available from, as of April 1, 2011: https://www.sigmaaldrich.com/safety-center/msds-search.html
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