CAS: 5240-72-2; Bicyclo[2.2.1]Heptan-2-Ylmethanol

该化合物是双环有机化合物,其独特结构由双环[2.2.1]heptane框架组成,附于环状系统的第二个碳(-CH2OH),该化合物一般是一种无色液体或固体,在室温下呈现中度的极性,因为存在可参与氢结合的氢氧化亚甲基组,其分子结构有助于其在有机合成中的潜在应用,并成为开发更复杂分子的建筑块.双环[2.2.1]七环衍生物对各个领域都感兴趣,包括医药化学和材料科学,因为它们独特的三维相容性和再活性.该化合物的稳定性和再活性可能受到诸如阻力和电子效应等因素的影响,使它成为理论化学和实验化学研究的课题.

结构式图片

相似化合物

824-62-4 19396-83-9 13137-31-0

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上下游产品

heptylmethyl acetate2-Bicyclo2.2.1heptylmethyl acetate methanol norborn-2-ene Methyl formate 2-iodomethyl-norbornane (3aS,6aS)-1,2,3,3a,4,6a-Hexahydro-pentalene heptylmethyl acetate2-Bicyclo2.2.1heptylmethyl acetate norbornane-2-carboxaldehyde

合成工艺路线路线简述

    📜5-降冰片烯-2-甲醇置于氢气体系中,用 乙醇 作为反应溶剂,以100%的收率获得产物2-降莰烷甲醇
    参考文献:人本构蛋白酶体β5C选择抑制剂的基于结构的设计.
    标题:人本构蛋白酶体β5C选择抑制剂的基于结构的设计.
    摘要:这项工作报告了人类组成型蛋白酶体β5C催化活性的高效和选择性抑制剂的发展.该工作描述了设计原理,即大疏水性p3残基和小疏水性p1残基,这些原理导致合成了一组肽环氧基酮;他们的评估和最有希望的化合物的选择,以进行进一步的分析.构效关系详细说明了随着化合物逐步多样化,β1C/ I,β2C/ I和β5I活性如何对抑制产生抗性.以顺式和反式的混合物形式获得了最有效的化合物-双环己基异构体和对映选择性合成解决了这个问题.与某些化合物复合的酵母蛋白酶体结构的研究为效力和特异性提供了理论依据.用最有效的化合物中的n末端替代更易溶的等同物会导致细胞渗透性分子选择性地和有效地阻断表达组成型蛋白酶体和免疫蛋白酶体的细胞中的β5C.
    DOI:10.1021/acs.Jmedchem.6B00705

    海关参考信息

    专利信息


    专利号:US-2002127598-A1
    优先权日:2000-03-27
    标题 :Solution-phase combinatorial library synthesis and pharmaceutically active compounds produced thereby
    发明人:ZHOU WENQIANG; UPENDRAN SATHYA; IYER RADHAKRISHNAN P
    摘要:The invention provides methods for solution-phase synthesis of nucleotide-based compounds and new libraries of such compounds. Compounds of the invention are useful for a variety of therapeutic applications, including treatment of viral or bacterial infections and associated diseases and disorders.

    专利号:US-6620796-B1
    优先权日:1999-11-08
    标题:Combinatorial library synthesis and pharmaceutically active compounds produced thereby
    发明人:ZHOU WENQIANG; JIN YI; ROLAND ARLENE; IYER RADHAKRISHNAN
    权利人:MICROLOGIX BIOTECH INC
    摘要:The invention provides new methods for synthesis of nucleotide-based compounds and new libraries of such compounds. Compounds of the invention are useful for a variety of therapeutic applications, including treatment of viral or bacterial infections and associated diseases and disorders.

    专利号:WO-2012163936-A1
    优先权日:2011-05-31
    标 题 :Process for the synthesis of benzotriazoles useful as uv-filters
    发明人:PRESCHEL MICHAEL; ROEDER MICHAEL; SCHLIFKE-POSCHALKO ALEXANDER; ZHANG KESHENG
    权利人:DSM IP ASSETS BV; PRESCHEL MICHAEL; ROEDER MICHAEL; SCHLIFKE-POSCHALKO ALEXANDER; ZHANG KESHENG
    摘要:The invention relates to an improved process for the manufacture of novel benzotriazoles as well to novel benzotriazoles obtained by the novel process. This novel economical process provides products in high purity and yields.

    专利号:WO-2010115869-A1
    优先权日:2009-04-03
    标 题 :Propofol phosphonyl derivatives, synthesis, and use in long acting formulations
    发明人:GONNISSEN YVES RENE JOHANNA PAUL
    权利人:SEPS PHARMA N V; GONNISSEN YVES RENE JOHANNA PAUL
    摘要:This invention relates to compounds represented by the structural formula (I), and the salts and stereoisomers thereof, wherein: - L is a linker selected from the group consisting of -(CH 2 ) P -O-, a single bond, formula (IA), -(CH 2 ) 1-8 -O-X(O)-, and - p is an integer from 1 to 8, - each R 3 and each R 4 is independently selected from the group consisting of C 1-20 alkyl, C 3-12 alkyl, C 3-12 cycloalkyl-C 1-4 alkyl, saturated heterocyclyl and saturated heterocyclyl-C 1-4 alkyl, and - X and Y are each independently C or S(O), - Z is selected from the group consisting of O, S(O) and NR 5 , - W is selected from the group consisting of halogen, OH, S(O)H and O - M + wherein M + is a monovalent cation; and - R 5 is selected from the group consisting of hydrogen and C 1-10 alkyl. These compounds are useful pharmaceutical agents with improved oral bioavailability.

    专利号:WO-2019143423-A1
    优先权日:2018-01-17
    标题:Flow controlled synthesis of bottlebrush macromolecules

    专利号:WO-9855085-A1
    优先权日:1997-06-04
    标题:Pharmaceutical compositions and methods
    发明人:BROWN DAVID A; KHORLIN ALEXANDER A; LESIAK KRYSTYNA; REN WU YUN
    权利人:CODON PHARMACEUTICALS INC; BROWN DAVID A; KHORLIN ALEXANDER A; LESIAK KRYSTYNA; REN WU YUN
    摘要:Disclosed are methods and compositions for regulating the melanin content of mammalian melanocytes; regulating pigmentation in mammalian skin, hair, wool or fur; treating or preventing various skin and proliferative disorders; increasing the differentiation of mammalian neuronal cells for purposes of treating neurodegenerative diseases or nerve damage; and stimulating cellular nitric oxide (NO) synthesis, cyclic guanosine monophosphate levels (cGMP), and protein kinase G (PKG) activity for purposes of treating diseases mediated by deficiencies in the NO/cGMP/PKG signal transduction pathway; by administration of various compounds, including alcohols, diols and/or triols and their analogues.

    供应商参考报价(招募中)

    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:Hari, Y.; Aoyama, T.; Shioiri, T., Science of Synthesis Knowledge Updates, (2010) 4, 30.
    摘要:Pesticide Index, Frear, E.H., ed., State College, PA, College Science Pub., 1969, 4(302), 1969
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