CAS: 95-77-2; 3,4-Dichlorophenol

上下游产品

CAS号1338215-36-3 [2-(3,4-dichlor... | CAS号1095223-19-0 1-(2-fluoro-pyr... | CAS号95-76-1 3,4-二氯苯胺 | CAS号95-50-1 邻二氯苯 | CAS号87-86-5 五氯苯酚 | CAS号1435-49-0 1,2-二氯-4-氟苯 | CAS号20555-91-3 3,4-二氯碘苯 | CAS号288-32-4 咪唑 | CAS号17847-51-7 3,4-Dichlorophe... | CAS号108-43-0 3-氯酚 | CAS号36404-30-5 3,4-二氯苯甲醚 | CAS号3428-24-8 4,5-二氯儿茶酚 | CAS号533-73-3 1,2,4-苯三酚 | CAS号3245-41-8 2-溴乙基-3,4-二氯苯基醚 | CAS号32022-41-6 2-(3,4-二氯苯氧基)乙酰肼 | CAS号39224-65-2 2-硝基-4,5二氯苯酚 | CAS号22532-80-5 3,4-DICHLOROPHE... | CAS号22526-30-3 4'',5''-dichlor... | CAS号21320-30-9 2-[(3,4-二氯苯氧基)甲... | CAS号95-57-8 邻氯苯酚

五氯酚置于fe/pd-Swy-2体系中,化学反应生成 3,4-二氯苯酚
参考文献:Synthesis Of Clay-Templated Subnano-Sized Zero Valent Iron (Zvi) Particles,Clays Containing Same,And Use Of Both In Contaminant Treatments
标题:Synthesis Of Clay-Templated Subnano-Sized Zero Valent Iron (Zvi) Particles,Clays Containing Same,And Use Of Both In Contaminant Treatments
摘要:提供一种黏土,其中包括具有负电荷位点的2:1 铝硅酸盐黏土,该2:1 铝硅酸盐黏土含有分布在黏土表面上的次纳米级零价铁(zvi)颗粒.在一个实施例中,至少一些或所有颗粒的横截面为五(5)埃或更小.还描述了合成方法以及新型黏土和黏土模板的次纳米尺度 Zvi 颗粒本身.这种新型产品在各种治理应用中很有用,包括用于还原和脱氯反应.

专利信息

专利号:US-10040752-B2
优先权日:2015-08-24
标 题 :Synthesis of levomethadone hydrochloride or dextromethadone hydrochloride and methods for use thereof
发明人：MKRTCHYAN GNEL; YAO QINGWEI
权利人:CODY LABORATORIES INC
摘要:Highly efficient methods for synthesis of levomethadone hydrochloride or dextromethadone hydrochloride are provided starting from D-alanine, or L-alanine, respectively, with retention of configuration. Methods for treating a subject are provided comprising administering a composition comprising an effective amount of levomethadone hydrochloride having not more than 10 ppm dextromethadone.

专利号:US-2004110228-A1
优先权日:2002-04-01
标 题:Combinatorial organic synthesis of unique biologically active compounds
发明人：MCALPINE SHELLI R; TAYLOR RACHEL E; BOLLA MEGAN L; SEGALL ANCA M
摘要:The invention provides a method for making a combinatorial library of cyclic compounds, such as Holliday junction-trapping compounds, comprising the steps of (a) obtaining a plurality of trimers according to the generic structure X 1- X 2- X 3 , wherein X 1 , X 2 and X 3 can be independently any naturally or nonnaturally occurring amino acids or peptidomimetics thereof; (b) optionally coupling a spacer S to the trimer at either end; (c) cyclizing two trimers or trimer-spacer conjugates in a head-to-tail orientation; thereby obtaining a combinatorial library of compounds, wherein the library does not include an unmodifed or naturally occurring Holliday Junction-trapping compounds. The invention additionally provides methods macrocyclic compounds that are synergimycin derivatives.

专利号:US-10647672-B2
优先权日:2017-10-03
标 题:Modulators of cell adhesion, methods and compositions therefor
发明人：BLASCHUK OREST WILLIAM
权利人:Zonula Incorporated; ZONULA INC
摘要:Compounds with activity as modulators of cell adhesion are disclosed. The compounds are derivatives of piperidin-4-amine. In some embodiments, a compound can be linked to a targeting agent, a pharmaceutically active substance and/or a support material. Methods for enhancing or inhibiting classical cadherin-mediated functions are also disclosed. The compounds can be used for the treatment or prevention of a variety of diseases including cancer. Compositions and devices, including skin patches comprising a compound are also disclosed. In addition, methods of synthesis of the compounds are provided.

专利号:US-6828466-B2
优先权日:2002-07-19
标题:Process for the synthesis of phenols from arenes
发明人：MALECZKA JR ROBERT E; SMITH III MILTON R; HOLMES DANIEL; SHI FENG
权利人:UNIV MICHIGAN STATE
摘要:A process to synthesize substituted phenols such as those of the general formula RR'R''Ar(OH) wherein R, R', and R'' are each independently hydrogen or any group which does not interfere in the process for synthesizing the substituted phenol including, but not limited to, halo, alkyl, alkoxy, carboxylic ester, amine, amide; and Ar is any variety of aryl or hetroaryl by means of oxidation of substituted arylboronic esters is described. In particular, a metal-catalyzed C-H activation/borylation reaction is described, which when followed by direct oxidation in a single or separate reaction vessel affords phenols without the need for any intermediate manipulations. More particularly, a process wherein Ir-catalyzed borylation of arenes using pinacolborane (HBPin) followed by oxidation of the intermediate arylboronic ester by OXONE is described.

专利号:US-RE35279-E
优先权日:1987-08-28
标题:Hydantoin derivatives
发明人：MOCHIDA EI; MURAKAMI KIMIHIRO; KATO KAZUO; KATO KATSUAKI; OKUDA JUN; MIWA ICHITOMO
权利人:MOCHIDA PHARM CO LTD
摘要:The present invention relates to novel hydantoin derivatives, processes for producing said hydantoin derivatives, pharmaceutical compositions containing at least one of said hydantoin derivatives as aldose reductase inhibitors and novel intermediate compounds in the synthesis of said hydantoin derivatives. The present invention is based on the selection of a hydantoin which is bonded by a sulfonyl group to various substituents at the 1-position of the hydantoin skeleton. The compounds of the present invention have a strong inhibitory activity against aldose reductase. These compounds are extremely useful for the treatment and/or prevention of various forms of diabetic complications based on the accumulation of polyol metabolites.

专利号:US-2019002394-A1
优先权日:2015-08-24
标 题 :Synthesis of levomethadone hydrochloride or dextromethadone hydrochloride and methods for use thereof