CAS: 56826-61-0; (2-Methylpyridine-3-yl)Methanol

该化合物是有机化合物,其特点是其环结构与甲基组和氢氧甲基组相替代,其特点是:环环为一甲基组和氢氧甲基组,该化合物为六人芳香环,含有一个氮原子,有助于其基本性和氢联结潜力; 氢氧甲基组(-CH2OH)的存在增强了其在极地溶剂中的溶解性,并允许其在氧化或酯化等各种化学反应中具有潜在的再活动; 环2位置的甲基组可影响该化合物的电子特性和阻塞性,影响其与其他分子的再活动及相互作用. (2-M-M-HIV-3-yl)乙醇可能展示生物活动,使其对医药化学和药物开发感兴趣. 其物理特性,如沸点,熔点和密度,通常通过实验方法确定,因为它们可以根据纯度和环境条件而变化.

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3222-56-8 65719-09-7 1721-26-2

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上下游产品

ethyl 2-methyl nicotinate 2-methyl-1,4-dihydro-pyridine-3-carboxylic acid ethyl ester methyl 2-methylnicotinate sodium hydrogencarbonate 3-methoxymethyl-2-methyl-pyridine 3-benzyloximethyl-2-methyl-pyridine 3-(bromomethyl)-2-methylpyridine 2-methyl-3-chloromethylpyridine hydr°Chloride

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    专利信息


    专利号:US-4546198-A
    优先权日:1983-01-18
    标 题 :Asymmetric synthesis of esters and acids
    发明人:STOUTAMIRE DONALD W
    权利人:SHELL OIL CO
    摘要:Stereoisomerically-enriched esters are prepared by treating a non-symmetrical ketene with a racemic or chiral tertiary-base-substituted alkylcarbinol. Optional hydrolysis of the esters gives the corresponding optically-active carboxylic acids corresponding to the non-symmetrical ketene.

    专利号:EP-1021457-B1
    优先权日:1996-07-05
    标题 :Method for the site specific synthesis of novel 3-hydroxypyridin-4(1h)-ones derivatives from aminoitols, products obtained by this method and their applications

    专利号:FR-2750699-A1
    优先权日:1996-07-05
    标 题:REGIOSPECIFIC SYNTHESIS OF NEW 3-HYDROXYPYDIRIN-4 (1H) -ONES DERIVATIVES FROM AMINOMONOSACCHARIDES OR AMINOITOLS. PRODUCTS OBTAINED BY THIS PROCESS AND THEIR APPLICATIONS

    专利号:WO-9725992-A1
    优先权日:1996-01-16
    标 题 :Tocolytic oxytocin receptor antagonists
    发明人:SPARKS MICHELLE A; FRIEDINGER ROGER M; PERLOW DEBRA S; WILLIAMS PETER D
    权利人:MERCK & CO INC; SPARKS MICHELLE A; FRIEDINGER ROGER M; PERLOW DEBRA S; WILLIAMS PETER D
    摘要:This invention relates to certain novel benzoxazinone compounds and derivatives thereof, their synthesis, and their use as oxytocin receptor antagonists. One application of these compounds is in the treatment of preterm labor. The ability of the compounds to relax uterine contractions in mammals also makes them useful for treating dysmenorrhea and stopping labor prior to cesarean delivery.

    专利号:CN-111646889-A
    优先权日:2020-04-29
    标题:Green Synthesis Method of Pharmaceutical Active Molecules GC-24 and Furugrelic Acid

    专利号:US-5726172-A
    优先权日:1996-01-16
    标题 :Tocolytic oxytocin receptor antagonists
    发明人:SPARKS MICHELLE A; FREIDINGER ROGER M; PERLOW DEBRA S; WILLIAMS PETER D
    权利人:MERCK & CO INC
    摘要:This invention relates to certain novel benzoxazinone compounds and derivatives thereof, their synthesis, and their use as oxytocin receptor antagonists. One application of these compounds is in the treatment of preterm labor. The ability of the compounds to relax uterine contractions in mammals also makes them useful for treating dysmenorrhea and stopping labor prior to cesarean delivery. A typical compound is as follows:

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    ✅ COA系统入驻 | 共享模式

    合成参考文献


    参考文献:10.1007/bf00639810
    参考文献:10.1007/bf00761096
    摘要:Trubnikov VI, Zhdanovich ES, Preobrazhenskii NA. Investigations in the field of pyridinecarboxylic acids. III. Gas-liquid chromatography in the production of nicotinic and isonicotinic acids from the β-picoline fraction. Pharmaceutical Chemistry Journal. 1968 Jan;2(1):27–9. doi: 10.1007/bf00761096.
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