CAS: 5182-44-5; 2-(3-Chlorophenyl)Ethanol

该化合物是一种有机化合物,其特征是存在一个附属于乙醇协会的氯联苯集团,该化合物一般是无色的,淡黄色液体,在水中具有中等溶性,同时在乙醇和乙醇等有机溶剂中具有良好的溶解性;氯原子存在于苯基环中,影响其化学反应,使其有可能成为各种化学反应的候选体,包括核生殖替代物和电药替代物;它显示出酒精的典型特性,例如形成氢结的能力,这可能影响其沸点和挥发性;此外,2-(3)-氯联苯基)乙醇可能被用于制药,农用化学品和有机合成的中间体;在处理和储存时,应参考安全数据,因为许多有机化合物,如果加入或吸入,它可能会对健康造成危害.

结构式图片

欧盟法规

ECHA物质C&L通报REACH预注册

上下游产品

CAS号1878-65-5 3-氯苯乙酸 | CAS号2039-85-2 3-氯苯乙烯 | CAS号766-83-6 3-氯苯乙炔 | CAS号53088-68-9 (3-氯苯基)乙酸甲酯 | CAS号75-21-8 环氧乙烷 | CAS号108-37-2 1-溴-3-氯苯 | CAS号18655-49-7 3-(3-氯苯基)-1-丙胺 | CAS号21640-47-1 3-(3-氯苯基)-丙腈 | CAS号52022-77-2 3-硝基苯乙醇 | CAS号34176-92-6 3-Chlorobibenzyl | CAS号16799-05-6 3-氯苯乙基溴 | CAS号791-28-6 三苯基氧化膦 | CAS号41904-40-9 3-氯苯乙醇 | CAS号5182-43-4 1-氯-3-(2-氯乙基)-苯

合成工艺路线路线简述

    3-氯苯乙烯置于水,E.Coli Bl21 Cells Expressing Styrene Monooxygenase Encoded On Plasmid Pet28A-Stya体系中,用 Aq. Phosphate Buffer 作为反应溶剂,化学反应 24.0H,以25%的收率获得产物3-氯苯乙醇
    参考文献:芳基烯烃的酶促对映选择性抗马尔科夫尼科夫水合
    标题:芳基烯烃的酶促对映选择性抗马尔科夫尼科夫水合
    摘要:苯乙烯单加氧酶催化芳基烯烃的对映选择性抗马尔科夫尼科夫水合,而不是环氧化,可以通过简单地从反应混合物中去除氧气来实现.具有类碳负离子中间体的酸碱机制使反应具有出色的抗马尔科夫尼科夫区域选择性.
    DOI:10.1002/anie.202206472

    海关参考信息

    专利信息


    专利号:US-2004053999-A1
    优先权日:1997-09-17
    标题 :Novel compounds and methods for synthesis and therapy
    发明人:BISCHOFBERGER NORBERT W; DAHL TERRENCE C; HITCHCOCK MICHAEL J M; KIM CHOUNG U; LEW WILLARD; LIU HONGTAO; MILLS ROGER G; WILLIAMS MATTHEW A
    摘要:Novel compounds are described. The compounds generally comprise an acidic group, a basic group, a substituted amino or N-acyl and a group having an optionally hydroxylated alkane moiety. Pharmaceutical compositions comprising the inhibitors of the invention are also described. Methods of inhibiting neuraminidase in samples suspected of containing neuraminidase are also described. Antigenic materials, polymers, antibodies, conjugates of the compounds of the invention with labels, and assay methods for detecting neuraminidase activity are also described.

    专利号:US-6225341-B1
    优先权日:1995-02-27
    标 题:Compounds and methods for synthesis and therapy
    发明人:BISCHOFBERGER NORBERT W; KIM CHOUNG U; LEW WILLARD; LIU HONGTAO; WILLIAMS MATTHEW A
    权利人:GILEAD SCIENCES INC
    摘要:Novel compounds are described. The compounds generally comprise an acidic group, a basic group, a substituted amino or N-acyl and a group having an optionally hydroxylated alkane moiety. Pharmaceutical compositions comprising the inhibitors of the invention are also described. Methods of inhibiting neuraminidase in samples suspected of containing neuraminidase are also described. Antigenic materials, polymers, antibodies, conjugates of the compounds of the invention with labels, and assay methods for detecting neuraminidase activity are also described.

    专利号:WO-2023183905-A2
    优先权日:2022-03-24
    标 题 :Deuterated analogs of pyrrole inhibitors of erk, synthesis thereof and intermediates thereto

    专利号:US-2005240034-A1
    优先权日:2002-05-07
    标 题 :Artemisinin-based peroxide compounds as broad spectrum anti-infective agents
    发明人:AVERY MITCHELL; MURALEEDHARAN KANNOTH M
    权利人:AVERY MITCHELL; MURALEEDHARAN KANNOTH M
    摘要:Described herein is the synthesis, bioassay results and utility of new C- 9 and C- 10 substituted artemisinin derivatives with easily functionalizable groups attached to the artemisinin skeleton through carbon chain or heteroatoms. Described also is the demonstration of this class of compounds for their broad-spectrum anti-parasitic activity. Certain of these analogs possess noticeable cytotoxicity deliberately focused on treatment of cancerous diseases.

    专利号:CN-107056630-A
    优先权日:2017-01-23
    标题 :A kind of indane derivative, its synthesis method and its application in medicine
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    合成参考文献


    摘要:Hay, M. B.; Hicks, J. D., Science of Synthesis: Cross Coupling and Heck-Type Reactions, (2012) 2, 141.
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