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2,3,5,6-Tetrafluoro-1,4-benzoquinone | CAS:527-21-9
2,3,5,6-Tetrafluoro-1,4-benzoquinone
  • 名称:2,3,5,6-四氟-1,4-苯醌 | 2,3,5,6-Tetrafluoro-1,4-benzoquinone
  • CAS号:527-21-9
  • 别名:2,3,5,6-Tetrafluoro-p-benzoquinone; Fluoranil; Fluoroanil; NSC 264881; Perfluoro-p-benzoquinone; Tetrafluoro-1,4-benzoquinone; Tetrafluoro-p-benzoquinone; Tetrafluoro-p-quinone; Tetrafluorobenzoquinone; p-Fluoranil
  • 分子式:C6F4O2
  • 分子量:180.06
  • EINESC号:208-411-9

产品描述

物理化学性质

熔点 185-189 ºC**
沸点 133.1±40.0 ºC (760 Tor
闪点 44.6±21.5 ºC, 计算值*
密度 1.62±0.1 g/cm3 (20 ºC

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SDS

来源 SDS样本
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Direct generation of acyclic polypropionate stereopolyads via double diastereo- and enantioselective iridium-catalyzed crotylation of 1,3-diols: beyond stepwise carbonyl addition in polyketide construction.Xin Gao et al.Journal of the American Chemical Society, 133(32), 12795-12800 (2011-07-12) Correlation of structure and activity in ansamycins: structure, conformation, and interactions of antibiotic rifamycin S.S K Arora Journal of medicinal chemistry, 28(8), 1099-1102 (1985-08-01) Chemical modification of the amide group of rifamycin S.M Taguchi et al.Chemical & pharmaceutical bulletin, 33(5), 2133-2136 (1985-05-01) Efficient strategy for the synthesis of stereopentad subunits of scytophycin, rifamycin S, and discodermolide.S BouzBouz et al.Organic letters, 3(25), 3995-3998 (2001-12-12) Characterization of rifamycin oxidase immobilized on alginate gel.U C Banerjee Biomaterials, artificial cells, and immobilization biotechnology : official journal of the International Society for Artificial Cells and Immobilization Biotechnology, 21(5), 675-683 (1993-01-01) Targeted mutagenesis of the Mycobacterium smegmatis mca gene, encoding a mycothiol-dependent detoxification protein.Mamta Rawat et al.Journal of bacteriology, 186(18), 6050-6058 (2004-09-03) Polyketide construction via hydrohydroxyalkylation and related alcohol C-H functionalizations: reinventing the chemistry of carbonyl addition.Anne-Marie R Dechert-Schmitt et al.Natural product reports, 31(4), 504-513 (2014-02-12) Detoxification of toxins by bacillithiol in Staphylococcus aureus.Gerald L Newton et al.Microbiology (Reading, England), 158(Pt 4), 1117-1126 (2012-01-21) Structure-activity relationships in open ansa-chain rifamycin S derivatives as inhibitors of HIV-1 reverse transcriptase.C Bartolucci et al.Farmaco (Societa chimica italiana : 1989), 50(9), 587-593 (1995-09-01) Enzymatic desymmetrization of a meso polyol corresponding to the C(19)-C(27) segment of rifamycin S.R Chênevert et al.The Journal of organic chemistry, 65(6), 1707-1709 (2000-04-06) Expeditious asymmetric synthesis of a stereoheptad corresponding to the C(19)-C(27)-ansa chain of rifamycins: formal total synthesis of Rifamycin S.Māris Turks et al.Chemistry (Weinheim an der Bergstrasse, Germany), 11(2), 465-476 (2004-11-20) Transformation of rifamycin S into rifamycins B and L. A revision of the current biosynthetic hypothesis.O Ghisalba et al.The Journal of antibiotics, 35(1), 74-80 (1982-01-01) Characterization of Mycobacterium tuberculosis mycothiol S-conjugate amidase.Micah Steffek et al.Biochemistry, 42(41), 12067-12076 (2003-10-15) Oxygen Enhancement of bactericidal activity of rifamycin SV on Escherichia coli and aerobic oxidation of rifamycin SV to rifamycin S catalyzed by manganous ions: the role of superoxide.Y Kono Journal of biochemistry, 91(1), 381-395 (1982-01-01) Molecular structure and conformation of rifamycin S, a potent inhibitor of DNA-dependent RNA polymerase.S K Arora et al.The Journal of antibiotics, 45(3), 428-431 (1992-03-01) Crotylboron-based synthesis of the polypropionate units of chaxamycins A/D, salinisporamycin, and rifamycin S.Ming Chen et al.The Journal of organic chemistry, 78(1), 3-8 (2012-06-19) Synthesis and structure-activity relationships of novel substituted 8-amino, 8-thio, and 1,8-pyrazole congeners of antitubercular rifamycin S and rifampin.Yafei Jin et al.Bioorganic & medicinal chemistry letters, 21(20), 6094-6099 (2011-09-10) 3-(Carboxyalkylthio) rifamycin S and SV derivatives inhibit human neutrophil functions.S Spisani et al.Inflammation, 22(5), 459-469 (1998-10-30) Studies on rifamycin oxidase immobilized on kappa-carrageenan gel.U C Banerjee Biomaterials, artificial cells, and immobilization biotechnology : official journal of the International Society for Artificial Cells and Immobilization Biotechnology, 21(5), 665-674 (1993-01-01) A comparative study of the redox-cycling of a quinone (rifamycin S) and a quinonimine (rifabutin) antibiotic by rat liver microsomes.D N Rao et al.Free radical biology & medicine, 22(3), 439-446 (1997-01-01) Solid state cultivation of Curvularia lunata for transformation of rifamycin B to S.A A Rasalkar et al.Indian journal of experimental biology, 40(8), 930-933 (2003-02-25) Rifamycin S and its geometric isomer produced by a newly found actinomycete, Micromonospora rifamycinica.Huiqin Huang et al.Antonie van Leeuwenhoek, 95(2), 143-148 (2009-01-07) Aerobic oxidation of rifamycin SV to rifamycin S catalyzed by horseradish peroxidase.Y Kono Journal of biochemistry, 91(5), 1789-1794 (1982-05-01) Transformation of rifamycin B with growing and resting cells of Curvularia lunata.U C Banerjee Enzyme and microbial technology, 15(12), 1037-1041 (1993-12-01) Oxabicyclo[3.2.1]octenes in organic synthesis--direct ring opening of oxabicyclo[3.2.1] systems employing silyl ketene acetals in concentrated solutions of lithium perchlorate-diethyl ether: application to the synthesis of the C(19)-C(27) fragment of rifamycin S.K W Hunt et al.Organic letters, 3(3), 481-484 (2001-06-29) NMR spectroscopic analysis of new spiro-piperidylrifamycins.Eduardo Rubio et al.Magnetic resonance in chemistry : MRC, 43(4), 269-282 (2005-01-28)
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