CAS: 23585-49-1; 3-(Hydroxymethyl)Pyrazole

该化合物是一个有机化合物,其特点是其配有五人环结构,含有两个相邻的氮原子的五人环;该化合物在配方环的三处,具有氢氧甲基组(-CH2OH),有助于其反应和各种化学反应的潜在应用;该化合物一般没有颜色,可粉黄的黄色液体或固体,视其纯度和形态而定;水氧化甲基组的存在,增强了其在极地溶剂中的溶液溶性,使其在有机合成中有用,并作为中间体用于生产药品和农用化学品;此外,1H-pyrazole-3-m乙醇可能展示生物活动,可加以探讨,以用于潜在的治疗用途;其稳定性和再活性可能受到诸如pH和温度等因素的影响,因此在实验室环境中在受控制的条件下处理它十分重要;

结构式图片

相似化合物

15366-34-4 3920-50-1 5932-27-4

欧盟法规

C&L通报

上下游产品

diazomethane diethyl ether propargyl alcohol 4,4-diethoxy-but-2-yn-1-ol 3-(chloromethyl)-1H-pyrazole 1-Amino-1H-pyrazol-3-methanol 3-bromomethylpyrazole 1-(7-(5-(hydroxymethyl)-1H-pyrazol-1-yl)-4-methoxy-1H-pyrrolo[2,3-c]pyridin-3-yl)-2-(5-(pyridin-2-yl)-3,4-dihydroisoquinolin-2(1H)-yl)ethane-1,2-dione

合成工艺路线路线简述

    吡唑-3-羧酸甲酯置于lithium Aluminium Tetrahydride体系中,用 四氢呋喃 用作溶剂,化学反应生成3-羟甲基吡唑
    参考文献:含吡唑亚基的大双环配体的合成:N,N'-联吡唑基隐窝
    标题:含吡唑亚基的大双环配体的合成:N,N'-联吡唑基隐窝
    摘要:吡唑基穴状配体[bpz.Bpz.Bpz](1)和[2.2.Bpz](2)是通过1,1'-联吡唑衍生物一步一步,非高稀释度的大环合成反应制得的.同样,描述了具有吡唑结构的三脚架配体(7)-(9).
    Doi:10.1039/c39850001765

    海关参考信息

    专利信息


    专利号:US-2005085555-A1
    优先权日:1997-08-21
    标 题:Composition, synthesis and therapeutic applications of polyamines
    发明人:MURPHY MICHAEL A; MALACHOWSKI MITCHELL R
    摘要:This invention relates to a process of synthesis and composition of open chain (ring), closed ring, linear branched and or substituted polyamines, polyamine derived tyrosine phosphatase inhibitors and PPAR partial agonists/partial antagonists via a series of substitution reactions and optimizing the bioavailability and biological activities of the compounds. Polyamines prevent the toxicty of neutoxins and diabetogenic toxins including paraquat, methyphenyl pyridine radical, rotenone, diazoxide, streptozotocin and alloxan. These polyamines can be to treat neurological, cardiovascular, endocrine acquired and inherited mitochondrial DNA damage diseases and other disorders in mammalian subjects, and more specifically to the therapy of Parkinson's disease, Alzheimer's disease, Lou Gehrig's disease, Binswanger's disease, Olivopontine Cerebellar Degeneration, Lewy Body disease, Diabetes, Stroke, Atherosclerosis, Myocardial Ischemia, Cardiomyopathy, Nephropathy, Ischemia, Glaucoma, Presbycussis, Cancer, Osteoporosis, Rheumatoid Arthritis, Inflammatory Bowel Disease, Multiple Sclerosis and as Antidotes to Toxin Exposure.

    专利号:US-2014057877-A1
    优先权日:2002-12-18
    标题:Therapeutic polyamine compositions and their synthesis
    发明人:MURPHY MICHAEL A; MALACHOWSKI MITCHELL R
    权利人:MURPHY MICHAEL A; MALACHOWSKI MITCHELL R
    摘要:This invention relates to a process of synthesis and composition of open chain (ring), closed ring, linear branched and or substituted polyamines, polyamine derived tyrosine phosphatase inhibitors and PPAR partial agonists/partial antagonists via a series of substitution reactions and optimizing the bioavailability and biological activities of the compounds. Polyamines prevent the toxicity of neurotoxins and diabetogenic toxins including paraquat, methyphenyl pyridine radical, rotenone, diazoxide, streptozotocin and alloxan. These polyamines can be utilized to treat neurological, cardiovascular, endocrine acquired and inherited mitochondrial DNA damage diseases and other disorders in mammalian subjects, and more specifically to the therapy of Parkinson's disease, Alzheimer's disease, Lou Gehrig's disease, Binswanger's disease, Olivopontine Cerebellar Degeneration, Lewy Body disease, Diabetes, Stroke, Atherosclerosis, Myocardial Ischemia, Cardiomyopathy, Nephropathy, Ischemia, Glaucoma, Presbycussis, Cancer, Osteoporosis, Rheumatoid Arthritis, Inflammatory Bowel Disease, Multiple Sclerosis and as Antidotes to Toxin Exposure.

    专利号:US-10874646-B2
    优先权日:2015-10-16
    标 题 :Epothilone analogs, methods of synthesis, methods of treatment, and drug conjugates thereof
    发明人:NICOLAOU KYRIACOS C; RHOADES DEREK; WANG YANPING; TOTOKOTSOPOULOS SOTIRIOS
    权利人:UNIV RICE WILLIAM M
    摘要:In one aspect, the present disclosure provides epothilone analogs of the formula (I) wherein the variables are as defined herein. In another aspect, the present disclosure also provides methods of preparing the compounds disclosed herein. In another aspect, the present disclosure also provides pharmaceutical compositions and methods of use of the compounds disclosed herein. Additionally, drug conjugates with cell targeting moieties of the compounds are also provided.

    专利号:US-9314021-B2
    优先权日:2004-11-03
    标题 :Formulations containing insect repellent compounds
    发明人:SCIALDONE MARK A
    权利人:DU PONT
    摘要:Dihydronepetalactone, a minor natural constituent of the essential oil of catmints ( Nepeta spp.) such as Nepeta cataria , has been identified as an effective insect repellent compound. Synthesis of dihydronepetalactone may be achieved by hydrogenation of nepetalactone, the major constituent of catmint essential oils. This compound, and compositions thereof, which also has fragrance properties, may be used commercially for its insect repellent properties.

    专利号:EP-0302633-A2
    优先权日:1987-08-07
    标 题:Beta-lactam compound, process for preparing the same, intermediate for synthesis of the same and medicinal composition for bacterially infectious disease therapy containing the same

    专利号:EP-3371176-A1
    优先权日:2015-10-16
    标 题:Epothilone analogs, methods of synthesis, methods of treatment, and drug conjugates thereof
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    合成参考文献


    参考文献:10.1134/s1070428025602791
    摘要:Belyaev DV, Chizhov DL, Rusinov GL, Charushin VN. Features of Synthesis of 5(3)-Polyfluoromethylpyrazole-3(5)-carbaldehydes and Their Dimethyl Acetals. Russ J Org Chem. 2025 Jun;61(6):1148–56. doi: 10.1134/s1070428025602791.
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