CAS: 117-12-4; 1,5-Dihydroxyanthraquinone

该化合物是高纯度炭疽衍生物,通常用作有机合成和染料生产的中间体,其主要优点包括:纯度达到85%,保证在诸如Vat染料制造和化学研究等应用中具有可靠的性能;复合物在普通有机溶剂中表现出极佳的热稳定性和溶解性,便于其在各种工业过程中使用;其分子结构允许进一步功能化,使其成为合成化学的多用途构件;该产品通常以精细粉形式供应,确保易于处理和反应混合物的统一分散;在干燥,凉爽条件下适当储存,长期保持稳定.

结构式图片

相似化合物

117-10-2 81-64-1 129-43-1

欧盟法规

ECHA物质C&L通报REACH预注册

上下游产品

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合成工艺路线路线简述

    蒽醌置于quicklime,硫酸,三氧化硫,水,Mercury(II) Oxide体系中,化学反应生成蒽绛酚
    参考文献:Schmidt,R. E.,Chemische Berichte,1904,Vol. 37,P. 69 Anm. 1
    标题:Schmidt,R. E.,Chemische Berichte,1904,Vol. 37,P. 69 Anm. 1

    海关参考信息

    专利信息


    专利号:US-3983145-A
    优先权日:1973-11-01
    标 题:Use of alpha-di(lower alkoxy) anthraquinones in the synthesis of Alizarin Saphirols
    发明人:WHITE DAVID L; FITZPATRICK JOSEPH W
    权利人:TOMS RIVER CHEMICAL CORP
    摘要:Alpha-dihydroxyanthraquinones used as intermediates in the synthesis of many dyestuffs, such as the Alizarin Saphirols (e.g. Color Constitution No. 63000, 63005, 63010, 63011, 63315 and 63610) can be replaced on an equimolar basis by alpha-di(lower alkoxy)anthraquinones. The alpha-di(lower alkoxy) anthraquinones can be converted in a single step, by treatment with oleum, to the corresponding alpha-dihydroxyanthraquinone-beta-disulfonic acids in almost quantitative yield. The corresponding diamine is obtained by dinitrating followed by reduction of the nitro groups. The known intermediate, leuco 1,4,5,8-tetrahydroxyanthraquinone (see C.I. No. 62500) can be obtained either by reduction of the diamine or by reduction of the dinitro compound. In one embodiment, the alpha-di(lower alkoxy)anthraquinone is obtained from dinitroanthraquinone by treatment thereof with methanol and KOH.

    专利号:US-6712949-B2
    优先权日:2001-07-22
    标 题:Electrochemical synthesis of hydrogen peroxide
    发明人:GOPAL RAMANATHAN
    权利人:ELECTROSYNTHESIS CO INC
    摘要:Improved methods and devices for the synthesis of hydrogen peroxide employing redox catalysts in a gas diffusion electrode or membrane electrode assembly in a semi-chemical/electrochemical system for the production of high purity, stable, usually acidic, aqueous solutions of peroxide at high conversion efficiencies without requiring organic solvents.

    专利号:US-2005009924-A1
    优先权日:2003-07-08
    标 题 :Synthesis and pharmaceuticals of novel bis-substituted anthraquinone derivatives
    发明人:HUANG HSU-SHAN
    摘要:This invention relates to novel anthraquinone compounds useful in the treatment of allergic, inflammatory conditions, antioxidant, tumor condition, stem cell application, tissue engineering, applied in treating age-associate tissue degeneration, reverse organ failure in chronic high-turnover disease and therapeutic compositions containing such compounds. The compounds of the present invention are 1,4-, 1,5- and 1,8-difunctionalized anthraquinones or analogs thereof. According to the practice of the invention, there are provided bis-symmetrical substituted anthraquinone compounds according to formula I: n n nwherein R1, R2, R3 and R4 present a straight, aminoalkylamino side chains or branched chain alkyl group having 1 to 6 carbons which may be substituted with one or more groups of R5, or R1, R2, R3 and R4 present phenyl or benzyl which may be substituted with one or two groups of R6; wherein R5 is selected from the group consisting of halogen, —RNH 2 , —RNH 2 R, —ROH, —NO 2 , —OCH 3 , —OCH 2 CH 3 , and —OCH 2 CH 2 CH 3 ; and wherein R6 is selected from the group consisting of a straight or branched chain alkyl group having 1 to 4 carbons, halogen, —RNH 2 , —RNH 2 R, —ROH, —NO 2 , —OCH 3 , —OCH 2 CH 3 , —OCH 2 CH 2 CH 3 , —CH 2 Br, —CH 2 Cl, —CH 2 OH, —C(CH 3 ) 3 , —(CH 2 ) 2 0H, —(CH 2 ) 3 OH, —(CH 2 ) 4 OH, —CH 2 NH 2 , —(CH 2 ) 2 NH 2 , —(CH 2 ) 3 NH 2 , —(CH 2 ) 4 NH 2 , —(CH 2 ) 5 NH 2 , —CH 2 N(CH 3 ) 2 , —(CH 2 ) 2 N(CH 3 ) 2 , —(CH 2 ) 2 NH(CH 2 ) 2 OH, —(CH 2 ) 3 NH(CH 2 ) 2 OH, —(CH 2 ) 2 NHCH 2 OH, —(CH 2 ) 3 NHCH 2 OH, —CH 2 CH(CH 3 ) 2 , —CHCl 2 , —CH(CH 3 )Cl, —(CH 2 ) 2 Cl, —(CH 2 ) 3 Cl, —(CH 2 ) 3 Br, —(CH 2 ) 4 Br, and —(CH 2 ) 4 Cl. n n Chart 1. Activation of hTERT promoter-driven SEAP expression by c-Myc. About 1×10 7 hTERT-BJ1 cells were transfected with 13.5 μg each of plasmid pSEAP or pPhTERT-SEAP and of plasmid pMT2T or pMT2T-cMyc by electroporation. After 24 h, viable cells were harvested, and reinoculated at a density of 3×10 5 /mL, and the SEAP activity after 24 h at 37 â–¡. The transfection efficiency of each experiment was determined by cotransfection with 1.5 μg of plasmid pCMVβ. The values were determined from three experiments. P<0.05 is presented by an asterisk.

    专利号:US-2003019758-A1
    优先权日:2001-07-22
    标 题 :Electrochemical synthesis of hydrogen peroxide

    专利号:WO-03010360-A1
    优先权日:2001-07-22
    标 题 :Electrochemical synthesis of hydrogen peroxide

    专利号:US-9917260-B2
    优先权日:2013-08-23
    标题 :Compounds with terminal heteroarylcyanovinylene groups and their use in organic solar cells
    发明人:SUNDARRAJ SUDHAKAR; EICKHOFF CHRISTIAN; BAHULAYAN SHEEJA; SEND ROBERT; NISHIMAE YUICHI; REICHELT HELMUT; TANABE JUNICHI; ERK PETER
    权利人:BASF SE
    摘要:The present invention relates to a photoactive material comprising a donor substance and an acceptor substance, wherein the donor substance comprises or consists of one or more compounds of formula (I) described herein, or the acceptor substance comprises or consists of one or more compounds of formula (I) described herein, or the donor substance comprises or consists of a first compound of formula (I) described herein and the acceptor substance comprises a second compound of formula (I) described herein with the proviso that the first and second compound are not the same, as well as to an organic solar cell comprising said photoactive material. The present invention also relates to a photoelectric conversion device comprising or consisting of two or more organic solar cells comprising said photoactive material and to compounds of formula (I) as described herein for use as donor substance or as acceptor substance in a photoactive material, Further, the present invention relates to the use of a compound of formula (III) as described herein in the synthesis of a compound of formula (I)as described herein.
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    主要参考文献


    1: Sharma J, Gupta R, Mishra S, Ramanujam K, Kulshrestha V. Sulfonated Poly(2,6-dimethyl-1,4-phenylene ether)-Modified Mixed-Matrix Bifunctional Polyelectrolyte Membranes for Long-Run Anthrarufin-Based Redox Flow Batteries. ACS Appl Mater Interfaces. 2023 Sep 27;15(38):44899-44911. doi: 10.1021/acsami.3c08089. Epub 2023 Sep 14. 11(36):33273-33284. doi: 10.1021/acsami.9b12455. Epub 2019 Aug 30. 15(6):4229-4235. doi: 10.1039/d4ra06418f.
    4: Rolta R, Yadav R, Salaria D, Trivedi S, Imran M, Sourirajan A, Baumler DJ, Dev K. In silico screening of hundred phytocompounds of ten medicinal plants as potential inhibitors of nucleocapsid phosphoprotein of COVID-19: an approach to prevent virus assembly. J Biomol Struct Dyn. 2021 Nov;39(18):7017-7034. doi: 10.1080/07391102.2020.1804457. Epub 2020 Aug 27.
    5: Nguyen TTH, Sin HJ, Pandey RP, Jung HJ, Liou K, Sohng JK. Biosynthesis of Rhamnosylated Anthraquinones in Escherichia coli. J Microbiol Biotechnol. 2020 Mar 28;30(3):398-403. doi: 10.4014/jmb.1911.11047.

    合成参考文献


    摘要:Schafer, E. W., Jr., W. A. Bowles Jr., and J. Hurlbut. 1983. The acute oral toxicity and repellency and hazard potential of 998 chemicals to one or more species of wild and domestic birds. Archives of Environmental Contamination and Toxicology 12:355-382.
    摘要:H. Gillet and J. C. Pariaud, Bull. Soc. Chim. Fr. 1966, 2624.
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