CAS: 97-24-5; 2,2'-Thiobis(4-Chlorophenol)

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CAS号106-48-9 对氯苯酚 | CAS号29097-31-2 Phenol,2,2'-sul... | CAS号13693-59-9 2,2-Dihydroxydi... | CAS号7647-01-0 盐酸 | CAS号64-19-7 冰醋酸 | CAS号75-15-0 二硫化碳 | CAS号3636-29-1 4-氯-2-[(5-氯-2-羟... | CAS号3161-15-7 2-bromo-6-(3-br... | CAS号13693-59-9 2,2-Dihydroxydi... | CAS号852-20-0 2,2'-thiobis[4-... | CAS号40654-56-6 4-chloro-2-(5-c...

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  • 29097-31-2 = 97-24-5
    反应条件:1.1 Reagents: Zinc Solvents: Acetic Acid
    标题:High Refractive Index Materials: A Structural Property Comparison Of Sulfide- And Sulfoxide-Containing Polyamides
    作者:Javadi,Ali; Abouzari-Lotf,Ebrahim; Mehdipour-Ataei,Shahram; Zakeri,Masoumeh; Nasef,Mohamed Mahmoud; Et Al
    参考文献:Journal Of Polymer Science 日期:2015 卷标:53(24) 页码:2867-2877]

    = 97-24-5
    反应条件:1.1 Reagents: Sulfur Dichloride
    标题:Synthesis And Spectral Studies Of Bis(2-Chloroethyl)Aminophosphoryl-Containing Compounds-Potential Anticancer Agents
    作者:Rao,L. Nagaprasada; Reddy,C. Devendranath; Reddy,V. Krishna; Hagar,Jacob D.; Tran,Kevin; Et Al
    参考文献:Phosphorus 日期:2002 卷标:177(2) 页码:399-410]

    = 97-24-5 [标题:Reaction Conditions
    标题:Study Of Some Problems In The Technology Of Production Of Oksid
    作者:Nekrasova,L. N.; Zetkin,V. I.; Sharov,V. G.; Tsvetkova,I. P.
    参考文献:V Sb. 日期:1975 卷标:(1975) 页码:102-5]

    = 97-24-5
    反应条件:1.1 Reagents: Ammonium Hydroxide Catalysts: Aluminum Chloride,Tin Tetrachloride Pentahydrate Solvents: Water; 24 H,Ph 8,Rt1.2 Catalysts: Ammonium Persulfate Solvents: Water1.3 Reagents: Sulfur,1-Dodecyl-3-Methylimidazolium Hexafluorophosphate; 10 H,Rt -> 110 °C
    标题:Process For Preparation Of Phenyl Sulfide In The Presence Of Solid Acid Catalyst
    参考文献:China]

    = 97-24-5
    反应条件:1.1 Reagents: Trichloroacetic Acid,Tetraethylammonium Perchlorate Solvents: Dichloromethane
    标题:Use Of A Sacrificial Sulfur Electrode In Electroorganic Chemistry. Iii. Formation Of The C-S-C Bond From Aromatic Ethers And Phenols
    作者:Elothmani,Driss; Do,Quang Tho; Simonet,Jacques; Le Guillanton,Georges
    参考文献:Bulletin De La Societe Chimique De France 日期:1994 卷标:131(7) 页码:779-88]

    = 97-24-5 [标题:Reaction Conditions
    标题:Preparation Of 2,2'-Thiobis(4-Chlorophenol)
    作者:Nekrasova,L. N.; Zetkin,V. I.; Sharov,V. G.; Tsvetkova,I. P.
    参考文献:Khimicheskaya Promyshlennost (Moscow 日期:1980 卷标:(1980)]

    = 97-24-5 [标题:Reaction Conditions
    标题:Development Of Oksid Preparation Technology
    作者:Afonin,L. P.; Bezrukova,N. A.; Volodin,N. L.; Erkov,V. V.; Voronin,Yu. A.; Et Al
    参考文献:V Sb. 日期:1975 卷标:(1975) 页码:37-40
2,2'-Sulfoxide-Bis(4-Chlorophenol)置于溶剂黄146,锌体系中,化学反应生成 2,2'-硫代双(4-氯苯酚)
参考文献:高折射率材料:含硫化物和亚砜的聚酰胺的结构性能比较
标题:高折射率材料:含硫化物和亚砜的聚酰胺的结构性能比较
摘要:高折射率聚酰胺(pas)是通过结合硫化物或亚砜键和氯取代基而开发的.通过两种新型二胺单体(2,2'-硫化物-双(4-氯-1-(4-氨基苯氧基))苯醚(3A)和2,2'-亚砜-双(4-)的缩聚反应合成pas.氯-1-(4-氨基苯氧基)苯醚(3B),带有各种芳族二酸(a-E),二胺单体中的邻硫醚或亚砜单元,氯侧基和柔性醚键赋予了所获得的pas在有机溶剂中具有极好的溶解性,反应生成的pa具有很高的热稳定性,在氮气中10%的失重温度超过415°C,在大气中超过399°C,氯取代基,硫化物或亚砜键和邻位的结合级联结构为聚合物提供了高透明度,在632.8 Nm处具有高达1.7401的高折射率值和低双折射(<0.0075).通过比较结果,还详细研究了含硫化物或亚砜键的类似pa的结构-性质关系.©2015 Wiley Periodicals,Inc. J. Polym.科学,A部分:Polym.化学 2015年,53,2867年至2877年
DOI:10.1002/pola.27764

海关参考信息

专利信息


专利号:US-6168931-B1
优先权日:1999-03-17
标题 :Enhanced in vitro synthesis of biological macromolecules using a novel ATP regeneration system
发明人:SWARTZ JAMES R; KIM DONG-MYUNG
权利人:UNIV LELAND STANFORD JUNIOR
摘要:Compositions and methods are provided for the enhanced in vitro synthesis of biological molecules where ATP is required for synthesis. Of particular interest is the synthesis of polymers, e.g. nucleic acids, polypeptides, and complex carbohydrates. A homeostatic system is used for production of ATP, where the required high energy phosphate bonds are generated in situ, e.g. through coupling with an oxidation reaction. The homeostatic energy source will typically lack high energy phosphate bonds itself, and will therefore utilize free phosphate in the reaction mix during generation of ATP. Since inorganic phosphate can be an inhibitory by-product of synthesis, the period of time when synthesis is maintained in vitro can be extended. The homeostatic energy source is provided in combination with an enzyme that catalyzes the creation of high energy phosphate bonds and with an enzyme that can use that high energy phosphate bond to regenerate ATP.

专利号:US-6994986-B2
优先权日:1999-03-17
标 题:In vitro synthesis of polypeptides by optimizing amino acid metabolism
发明人:SWARTZ JAMES ROBERT; KIM DONG-MYUNG
权利人:UNIV LELAND STANFORD JUNIOR
摘要:Compositions and methods are provided for the enhanced in vitro synthesis of polypeptides. In order to improve the performance of in vitro protein synthesis reactions, metabolic inhibitors, or manipulation of a source organism, is used to diminish or avoid the action of enzymes responsible for undesirable amino acids production or depletion. A homeostatic system may be used for production of ATP, where the required high energy phosphate bonds are generated in situ, e.g. through coupling with an oxidation reaction. The homeostatic energy source will typically lack high energy phosphate bonds itself, and will therefore utilize free phosphate in the reaction mix during generation of ATP. The homeostatic energy source is provided in combination with an enzyme that catalyzes the creation of high energy phosphate bonds and with an enzyme that can use that high energy phosphate bond to regenerate ATP.

专利号:US-2011195450-A1
优先权日:2005-09-27
标 题 :In Vitro Protein Synthesis Systems for Membrane Proteins that Include Adolipoproteins and Phospholipid Adolipoprotein Particles
发明人:KUDLICKI WIESLAW; FLETCHER JULIA; KATZEN FEDERICO
权利人:LIFE TECHNOLOGIES CORP
摘要:In vitro protein synthesis systems and methods are provided that produce membrane proteins in soluble form. In some aspects, the invention provides methods of synthesizing proteins using in vitro protein synthesis systems that include an apolipoprotein, in which higher yields of soluble protein are produced than in the absence of the apolipoprotein. Apolipoproteins useful in the present invention include naturally occurring apolipoproteins, as well as sequence variants of wild-type apolipoproteins, and engineered apolipoproteins. The apolipoproteins can be provided in an in vitro protein synthesis system associated with lipid or not associated with lipid. The invention also provides compositions and kits for synthesis of proteins in soluble form, in which the compositions and kits include cell extracts for protein translation and at least one apolipoprotein biomolecule.

专利号:US-6337191-B1
优先权日:1999-03-22
标 题:Vitro protein synthesis using glycolytic intermediates as an energy source
发明人:SWARTZ JAMES; KIM DONG-MYUNG
权利人:UNIV LELAND STANFORD JUNIOR
摘要:Compositions and methods are provided for the enhanced in vitro synthesis of biological molecules where ATP is required for synthesis. Of particular interest is the synthesis of polymers, e.g. nucleic acids, polypeptides, and complex carbohydrates. Glycolytic intermediates or glucose are used as an energy source, in combination with added NADH or NAD + .

专利号:WO-2007038755-A1
优先权日:2005-09-27
标 题:In vitro protein synthesis systems for membrane proteins that include apolipoproteins and phospholipid-apolipoprotein particles
发明人:KUDLICKI WIESLAW; FLETCHER JULIA; KATZEN FEDERICO
权利人:INVITROGEN CORP; KUDLICKI WIESLAW; FLETCHER JULIA; KATZEN FEDERICO
摘要:In vitro protein synthesis systems and methods are provided that produce membrane proteins in soluble form. In some aspects, the invention provides methods of synthesizing proteins using in vitro protein synthesis systems that include an apolipoprotein, in which higher yields of soluble protein are produced than in the absence of the apolipoprotein. Apolipoproteins useful in the present invention include naturally occurring apolipoproteins, as well as sequence variants of wild-type apolipoproteins, and engineered apolipoproteins. The apolipoproteins can be provided in an in vitro protein synthesis system associated with lipid or not associated with lipid. The invention also provides compositions and kits for synthesis of proteins in soluble form, in which the compositions and kits include cell extracts for protein translation and at least one apolipoprotein biomolecule.

专利号:US-6699981-B2
优先权日:1999-09-22
标题 :Method and compositions for improved polynucleotide synthesis
发明人:YANG SHUWEI
权利人:GENECOPOEIA INC
摘要:The sensitivity and specificity of polynucleotide synthesis is increased by protecting the 3'-end of an oligonucleotide used as a primer in the synthesis of the polynucleotide. Protection of the 3'-end of an oligonucleotide prevents non-specific chain elongation. Removal of blocking group an elevated temperature, using a thermostable enzyme, permits template-specific polynucleotide synthesis. The present invention also provides oligonucleotides with a 3' end protected by a blocking group and a thermostable enzyme capable of removing the blocking group at an elevated temperature. The compositions and methods of the invention are very useful in a variety of techniques for DNA/RNA amplification and analysis, including medical genetics research and diagnosis, pathogen detection, forensic, and animal and plant genetics applications, among others.
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1: Hinoshita M, Abe T, Sato A, Maeda Y, Takeyoshi M. False-negative chemicals in ESR-based photosafety test (ESR-PT) and their significance for photosafety evaluations: examples of bithionol, fenticlor and cilnidipine. J Toxicol Sci. 2022;47(12):503-506. doi: 10.2131/jts.47.503. 26(9):409-12. 95(3):287-91. 2(5918):556-7. doi: 10.1136/bmj.2.5918.556-c.
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12: Hinoshita M, Abe T, Sato A, Maeda Y, Takeyoshi M. Modified ESR-based photosafety test (ESR-PT) detecting singlet oxygen and free radical formation. J Appl Toxicol. 2023 Dec 6. doi: 10.1002/jat.4569. Epub ahead of print. 98(2):96-101. Spanish. 28(6):186-9. German. 2(5):371-5. doi: 10.1016/0923-1811(91)90031-r. 119(12):983-5. French.

合成参考文献


参考文献:10.1104/pp.109.148742
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参考文献:10.2174/1875397301105010030
摘要:Sexton JZ, Danshina PV, Lamson DR, Hughes M, House AJ, Yeh L, O’Brien DA, Williams KP. Development and Implementation of a High Throughput Screen for the Human Sperm-Specific Isoform of Glyceraldehyde 3-Phosphate Dehydrogenase (GAPDHS). Curr Chem Genomics. 2011 Jul 04;5():30–41. doi: 10.2174/1875397301105010030.
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