CAS: 51512-09-5; 2-Chlorophenylacetyl Chloride (Stabilized With Copper Chip)

该化合物是一种该化合物是一种反应式氯乙烯组,能够与氨和酒精等核素产生有效的相互碰撞反应;其2-氯苯基混合物会提高电益益益,有助于将2-氯苯乙基酯组引入目标分子;该化合物对于制作β-林丹,除草剂和其他精密化学品特别宝贵;在受控制条件下,该化合物表现出高度纯度和稳定性,确保合成应用的一贯性能;由于其湿度敏感度和腐蚀性,适当处理至关重要;建议惰性大气中的储存保持回活性.

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CAS号2444-36-2 2-氯苯乙酸 | CAS号79-37-8 草酰氯 | CAS号609-65-4 邻氯苯甲酰氯 | CAS号118-91-2 邻氯苯甲酸 | CAS号492-97-7 2,2'-双噻吩 | CAS号21193-23-7 1-(2-chlorophen... | CAS号2184-85-2 2-(2-氯苯基)丙酸 | CAS号2050-67-1 3,3'-二氯联苯 | CAS号717910-62-8 3,2'-dichloro-d... | CAS号85259-19-4 α-溴-氯苯乙酸甲酯 | CAS号82302-27-0 8-氯-Β-四氢萘酮 | CAS号6305-95-9 2-氯苯基丙酮 | CAS号10268-06-1 2-(2-氯苯基)乙酰胺

合成工艺路线路线简述

    1-(2-Chlorophenyl)-2-Diazoethanone置于草酰氯,N,N-二甲基甲酰胺,Silver(L) Oxide体系中,用 1,4-二氧六环,二氯甲烷 作为反应溶剂,化学反应生成 2-氯苯基乙酰氯
    参考文献:Quinolones As Gonadotropin Releasing Hormone (Gnrh) Antagonists: Simultaneous Optimization Of The C(3)-Aryl And C(6)-Substituents
    标题:Quinolones As Gonadotropin Releasing Hormone (Gnrh) Antagonists: Simultaneous Optimization Of The C(3)-Aryl And C(6)-Substituents
    摘要:A Series Of 3-Arylquinolones Was Prepared And Evaluated For Their Ability To Act As Gonadotropin Releasing Hormone (Gnrh) Antagonists. A Variety Of Substitution Patterns Of The 3-Aryl Substituent Are Described. The 3,4,5-Trimethylphenyl Substituent (23H) Was Found To He Optimal. (C) 2000 Elsevier Science Ltd. All Rights Reserved.
    DOI:10.1016/s0960-894X(00)00318-8

    海关参考信息

    专利信息


    专利号:WO-9700244-A1
    优先权日:1995-06-19
    标题 :Process for parallel synthesis of a non-peptide library
    发明人:FRITZ JAMES E; KALDOR STEPHEN W
    权利人:LILLY CO ELI; FRITZ JAMES E; KALDOR STEPHEN W
    摘要:A process for the sequential preparation of a library of compounds having pharmaceutical usage. The process involves the sequential mixing of solution phase reagents, followed by scavenging of excess unreacted reagents with solid phase scavenging agents. The process is highly iterative and applicable for producing various ureas, thiureas, amides, carbonates and tertiary amines.

    专利号:RU-2014330-C1
    优先权日:1988-05-23
    标题:Method of synthesis of 1,2,3,4-tetrahydronaphthalene derivatives or their pharmaceutically acceptable acid-additive salt

    专利号:US-7585875-B2
    优先权日:2006-06-06
    标 题 :Substituted pyrazolo[1,5-a]pyridine compounds and their methods of use
    发明人:GAETA FEDERICO C A; GROSS MATTHEW; JOHNSON KIRK W
    权利人:AVIGEN INC
    摘要:The present invention is directed to substituted pyrazolo[1,5-a]pyridines and related methods for their synthesis and use.

    专利号:US-4113946-A
    优先权日:1975-01-02
    标题:Δ2,3 -1,4-Morpholine-2-carboxylic acid derivatives as antibacterial agents
    发明人:BELLEAU BERNARD R; DOYLE TERRENCE W; LUH BING YU; CONWAY TERRY T
    权利人:BRISTOL MYERS CO
    摘要:There is described the stereoselective total synthesis by a variety of routes of novel suitably substituted Δ 2 ,3 -1,4-morpholine-2-carboxylic acids possessing a fused β-lactam ring in the 1,6-position and carrying a substituent cis to carbon 5 in the 7-position of the fused ring system represented by the general formula ##STR1## wherein Q is hydrogen, alkyl, aralkyl or --CH 2 COOZ where Z is hydrogen or the residue of an ester group and X is amino, azido or acylamino. Also included in the invention are compounds of the above formula in which the carboxyl group at the 2-position is protected as by an easily cleavable ester group and salts of both the free acids and carboxyl-protected compounds. Those compounds in which X is acylamino and their physiologically hydrolyzed esters and pharmaceutically acceptable salts are potent antibacterial agents.

    专利号:UA-79448-C2
    优先权日:2002-02-06
    标题 :Derivatives of 3-aryl-2,5-dihydroxy-1,4-benzoquinone, method for synthesis and pharmaceutical composition

    专利号:CN-108863774-A
    优先权日:2018-06-09
    标 题 :A kind of method of 2,4-dichlorophenylacetyl chloride synthesis
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    合成参考文献


    摘要:Tidwell, T. T., Science of Synthesis, (2006) 23, 396.
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