CAS: 694-82-6; α-Fluorocyclohexanone

该化合物是含有分子式C6H9FO的氟化环烷,该化合物对合成有机化学感兴趣,因为存在反应性碳基组和氟替代体,可影响其反应性和稳定性.氟原子会增强α-碳的电益性,使其在核生殖替代和氟反应方面有用.其环己酮骨干为制药和农用化学中间体的进一步功能化提供了多功能的手架.该化合物的界定明确的结构和纯度使其适合研究应用,特别是用于开发用于生物活性分子的氟化模拟.

结构式图片

相似化合物

292150-03-9 75024-00-9 14365-32-3

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合成工艺路线路线简述

    📜1-环己烯氧基三甲基硅烷置于三氟甲磺酸n-吡啶鎓体系中,用 二氯甲烷 作为反应溶剂,化学反应 7.0H,以87%的收率获得产物2-氟环己酮
    参考文献:N-氟吡啶鎓三氟甲磺酸盐及其衍生物:有用的氟化剂
    标题:N-氟吡啶鎓三氟甲磺酸盐及其衍生物:有用的氟化剂
    摘要:N-氟吡啶鎓三氟甲磺酸盐及其衍生物,稳定且不吸湿的晶体,被广泛用作轻度和选择性氟化各种有机化合物的试剂.
    DOI:10.1016/s0040-4039(00)84980-1

    海关参考信息

    专利信息


    专利号:US-4215044-A
    优先权日:1979-04-23
    标题:Synthesis of α-fluorocarbonyl compounds
    发明人:MIDDLETON WILLIAM J
    权利人:DU PONT
    摘要:Process for preparing an organic compound of the formula R 2 R 2 CFC(O)R 3 , which process comprises contacting and reacting in a reaction mixture which includes an inert solvent, at a temperature of -40° C. to -100° C., ROF and ##STR1## R is polyfluoroperhaloalkyl of 1-6 carbon atoms or FOCF 2 ; R 1 is hydrocarbyl of 1-6 carbon atoms; n each R 2 is selected from H, alkyl of 1-17 carbon atoms, cycloalkyl of 3-6 carbon atoms, aryl, heteroaryl and such alkyl, cycloalkyl, aryl and heteroaryl substituted by halogen or alkoxy of 1-6 carbon atoms; n R 3 is selected from H, alkyl and haloalkyl of 1-16 carbon atoms, cycloalkyl of 3-10 carbon atoms, aryl and haloaryl, OSi(R 1 ) 3 , OH, NH 2 , alkoxy of 1-6 carbon atoms, aryloxy, NHR 1 and NR 1 2 wherein R 1 is alkyl of 1-6 carbon atoms, N-arylamino and nitrogen or sulfur heterocyclic of 4-5 carbon atoms; n R 3 and one R 2 taken together is a diradical which with the Câ•?C group is carbocyclic, heterocyclic or haloheterocyclic, and recovering from the reaction mixture the compound of the formula R 2 R 2 CFC()R 3 .

    专利号:US-9073935-B2
    优先权日:2011-11-11
    标 题:Substituted benzylspiroindolin-2-one analogs as positive allosteric modulators of the muscarinic acetylcholine receptor M1
    发明人:LINDSLEY CRAIG W; CONN P JEFFREY; WOOD MICHAEL R; HOPKINS COREY R; MELANCON BRUCE J; POSLUSNEY MICHAEL S
    权利人:UNIV VANDERBILT
    摘要:In one aspect, the invention relates to substituted benzylspiroindolin-2-one analogs compounds, derivatives thereof, and related compounds, which are useful as positive allosteric modulators of the muscarinic acetylcholine receptor M 1 (mAChR M 1 ); synthesis methods for making the compounds; pharmaceutical compositions comprising the compounds; and methods of treating neurological and psychiatric disorders associated with muscarinic acetylcholine receptor dysfunction using the compounds and compositions. This abstract is intended as a scanning tool for purposes of searching in the particular art and is not intended to be limiting of the present invention.

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    品牌试剂参考报价(招募中)

    📌 第三方产品分析报告

    ✅ COA系统入驻 | 共享模式

    合成参考文献


    摘要:Yamazaki, T., Science of Synthesis Knowledge Updates, (2017) 2, 316.
    摘要:Xie, J.-H.; Zhou, Q.-L., Science of Synthesis, (2022) , 414.
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