合成目标产物 Disperse Red 9 主要起始原料 Tetrabutylammonium Bromide And 1-Aminoanthraquinone And Dimethyl Sulfate
82-34-8 = 82-38-2 反应条件:1.1 Reagents: Urea,Calcium Hydroxide Solvents: Xylene,Water; Rt -> 120 °C; 4 H,0.24 Mpa,120 °C1.2 Reagents: Hydrochloric Acid,Ammonium Chloride Solvents: Water 标题:Synthesis Of 1-Methylaminoanthraquinone 作者:Yu,Hong-Xia; Et Al 参考文献:Ranliao Yu Ranse 日期:2003 卷标:40(1)]
82-44-0 = 82-38-2 反应条件:1.1 Reagents: Copper Solvents: Pyridine,Water 标题:Latest Tests In Control Of Tomato Anthracnose 作者:Runnells,H. A.; Et Al 参考文献:Farm & Home Research 日期:1949 卷标:34 页码:67-70]
82-44-0 = 82-38-2 反应条件:1.1 Reagents: Cuprous Chloride 标题:Copper-Catalyzed Amination Of α-Substituted Anthraquinones 作者:Yoshida,Katsuhira; Et Al 参考文献:Chemistry Letters 日期:1978 卷标:(7) 页码:765-8]
82-45-1 = 82-38-2 反应条件:1.1 Solvents: 1-Propyl-3-Methylimidazolium Bromide; 6 H,120 °C 标题:Ionic Liquids As Novel And Recyclable Reaction Media For N-Alkylation Of Amino-9,10-Anthraquinones By Trialkyl Phosphites 作者:Yavari,Issa; Et Al 参考文献:Tetrahedron Letters 日期:2007 卷标:48(21) 页码:3753-3756]
680-31-9 + 82-44-0 = 82-38-2 [标题:Reaction Conditions 标题:Reactions Of 1,5-Dichloroanthraquinone With Nucleophiles 作者:Ruediger,Edward H.; Et Al 参考文献:Journal Of Organic Chemistry 日期:1980 卷标:45(10) 页码:1974-8]
84-65-1 = 82-38-2 [标题:Reaction Conditions 标题:Photoamination Reaction Of 9,10-Anthraquinone 作者:Loskutov,V. A.; Et Al 参考文献:Izvestiya Sibirskogo Otdeleniya Akademii Nauk Sssr 日期:1978 卷标:(4) 页码:135-7]
82-44-0 + 123-39-7 = 82-38-2 反应条件:1.1 Catalysts: Ethanolamine 标题:Anomalous Halogen To Dimethylamino Replacement With N,N-Dimethylformamide Catalyzed By Ethylenediamine Or 2-Aminoethanol 作者:Yamamoto,Hiroshi 参考文献:Bulletin Of The Chemical Society Of Japan 日期:1982 卷标:55(8) 页码:2685-6]
128-67-6 = 82-38-2 [标题:Reaction Conditions 标题:1-Methylamino-2,4-Dibromoanthraquinone 作者:Ufimtsev,V. N.; Et Al 参考文献:Zhurnal Vsesoyuznogo Khimicheskogo Obshchestva Im. D. I. Mendeleeva 日期:1976 卷标:21(4) 页码:467-8]
73178-74-2 = 82-38-2 反应条件:1.1 Reagents: Potassium Amide 标题:Reactions Of 1,5-Dichloroanthraquinone With Nucleophiles 作者:Ruediger,Edward H.; Et Al 参考文献:Journal Of Organic Chemistry 日期:1980 卷标:45(10) 页码:1974-8]
82-34-8 = 82-38-2 反应条件:1.1 Reagents: Methylamine Solvents: Isoamyl Alcohol 标题:Reaction Of 1-Chloro- And 1-Nitroanthraquinones With 3-(Alkylamino)- And 3-(Dialkylamino)Propionitriles 作者:Vostrova,V. N.; Et Al 参考文献:Zhurnal Organicheskoi Khimii 日期:1986 卷标:22(5) 页码:1046-9]
3571-23-1 = 82-38-2 反应条件:1.1 Reagents: Potassium Carbonate,Sodium Hydroxide,Tetrabutylammonium Hydrogen Sulfate Solvents: Toluene1.2 - 标题:Facile Synthesis Of Substituted N-Monoalkylaromatic Amines Under Phase-Transfer Catalysis Conditions 作者:Kalkote,U. R.; Et Al 参考文献:Synthetic Communications 日期:1991 卷标:21(18-19) 页码:1889-900]
82-44-0 = 82-38-2 反应条件:1.1 Reagents: Potassium Acetate Solvents: Water 标题:Manufacture Of 1-(Alkylamino)Anthraquinones For Dyes In High Yield And Purity 参考文献:Japan]
82-45-1 = 82-38-2 反应条件:1.1 Reagents: Potassium Carbonate,Sodium Hydroxide Catalysts: Tetrabutylammonium Bromide 标题:Phase Transfer Catalyzed N-Monoalkylation Of Aminoanthraquinones 作者:Ramrao,Kalkote Uttam; Et Al 参考文献:Synthetic Communications 日期:1991 卷标:21(10-11) 页码:1129-35]
82-34-8 + 693-05-0 = 82-38-2 反应条件:1.1 Solvents: 1-Butanol 标题:Reaction Of 1-Chloro- And 1-Nitroanthraquinones With 3-(Alkylamino)- And 3-(Dialkylamino)Propionitriles 作者:Vostrova,V. N.; Et Al 参考文献:Zhurnal Organicheskoi Khimii 日期:1986 卷标:22(5) 页码:1046-9]
5960-55-4 = 82-38-2 [标题:Reaction Conditions 标题:Photochemical Substitution Of Amino- And Hydroxyanthraquinones 作者:Hamilton,Kenneth; Et Al 参考文献:Journal Of The Chemical Society 日期:1980 卷标:(10) 页码:1544-8]
82-44-0 + 693-05-0 = 82-38-2 反应条件:1.1 Solvents: Methanol 标题:Reaction Of 1-Chloro- And 1-Nitroanthraquinones With 3-(Alkylamino)- And 3-(Dialkylamino)Propionitriles 作者:Vostrova,V. N.; Et Al 参考文献:Zhurnal Organicheskoi Khimii 日期:1986 卷标:22(5) 页码:1046-9]
52868-88-9 = 82-38-2 反应条件:1.1 Reagents: Sodium Chlorate 标题:1-Methylaminoanthraquinone 作者:Wilson,C. V.; Et Al 参考文献:Organic Syntheses 日期:1949 卷标:29 页码:66-8]
= 82-38-2 [标题:Reaction Conditions 标题:Photolysis Of (Nitrosomethylamino)Anthraquinones 作者:Klimenko,L. S.; Et Al 参考文献:Izvestiya Akademii Nauk Sssr 日期:1991 卷标:(9) 页码:2098-102]
82-46-2 + 123-39-7 = 82-38-2 反应条件:1.1 -2.1 Reagents: Potassium Amide 标题:Reactions Of 1,5-Dichloroanthraquinone With Nucleophiles 作者:Ruediger,Edward H.; Et Al 参考文献:Journal Of Organic Chemistry 日期:1980 卷标:45(10) 页码:1974-8]
680-31-9 + 82-46-2 = 82-38-2 反应条件:1.1 -2.1 Reagents: Potassium Amide 标题:Reactions Of 1,5-Dichloroanthraquinone With Nucleophiles 作者:Ruediger,Edward H.; Et Al 参考文献:Journal Of Organic Chemistry 日期:1980 卷标:45(10) 页码:1974-8
专利号:US-6596884-B2 优先权日:1998-06-29 标 题:Synthesis of hydrogen peroxide 发明人:BECKMAN ERIC J; HANCU DAN 权利人:UNIV PITTSBURGH 摘要:A method for synthesizing hydrogen peroxide comprises the steps of: synthesizing an analog of anthraquinone that is miscible or soluble in carbon dioxide; reacting the analog of anthraquinone with hydrogen in carbon dioxide to produce a corresponding analog of tetrahydroquinone; and reacting the analog of tetrahydroquinone with oxygen to produce the hydrogen peroxide and regenerate the analog of anthraquinone. A chemical compound having the formula: n wherein R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , R 7 , and R 8 are independently, the same or different, H, R C , or R S R C , wherein R S is a spacer group and R C is a fluoroalkyl group, a fluoroether group, a silicone group, an alkylene oxide group, a fluorinated acrylate group, or a phosphazine group, and wherein at least one of R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , R 7 , and R 8 is not H.
专利号:US-6342196-B2 优先权日:1998-06-29 标题 :Synthesis of hydrogen peroxide
专利号:US-2002110516-A1 优先权日:1998-06-29 标题:Synthesis of hydrogen peroxide
专利号:WO-0000428-A1 优先权日:1998-06-29 标题:Synthesis of hydrogen peroxide
专利号:US-2001007045-A1 优先权日:1998-06-29 标 题 :Synthesis of hydrogen peroxide
专利号:RU-2059611-C1 优先权日:1993-02-04 标 题 :Method of 4-bromo-1-methylaminoanthraquinone synthesis
[参考文献]: T C Marrs, Et Al. Inhalation Toxicity Of A Smoke Containing Solvent Yellow 33, Disperse Red 9 And Solvent Green 3 In Laboratory Animals. Hum Toxicol. 1984 Aug;3(4):289-308.
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. 参考文献:10.1007/s10895-006-0093-9 摘要:Umadevi M, Vanelle P, Terme T, Ramakrishnan V. Spectral investigations on 2,3-bis(chloromethyl)-1,4- anthraquinone: solvent effects and host–guest interactions. Journal of Fluorescence. 2006 Jun 15;16(4):569–79. doi: 10.1007/s10895-006-0093-9.