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hept-2-yne-1,7-diol | 207980-27-6

中文名称
——
中文别名
——
英文名称
hept-2-yne-1,7-diol
英文别名
Hept-2-in-1,7-diol
hept-2-yne-1,7-diol化学式
CAS
207980-27-6
化学式
C7H12O2
mdl
——
分子量
128.171
InChiKey
YILMJSBHWCLMLW-UHFFFAOYSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

计算性质

  • 辛醇/水分配系数(LogP):
    0.1
  • 重原子数:
    9
  • 可旋转键数:
    3
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.71
  • 拓扑面积:
    40.5
  • 氢给体数:
    2
  • 氢受体数:
    2

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量
  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    hept-2-yne-1,7-diol 在 Jones reagent 作用下, 以 丙酮 为溶剂, 反应 1.0h, 生成 7-hydroxy-hept-2-ynoic acid
    参考文献:
    名称:
    Triynes的苯并环生成通过自发掺入亲核试剂产生功能化的芳烃。
    摘要:
    酯束缚的1,3,8-三炔的热反应提供了新的苯并环氧基化产物,并伴随有亲核试剂的结合。有证据表明,该反应是通过第一步中的Alder-ene反应生成的Allene-Enyne中间体进行的。根据丙二烯-烯炔中间体上炔基部分的取代基,后续的转化可采用两种不同的途径之一,每种途径可导致不连续的芳构化产物。硅烷取代的1,3,8-三炔的苯并环形成芳烃产品,并在新形成的苯核上掺入了亲核试剂,而芳基取代基导致亲核试剂捕获在与芳基取代基相连的苄基碳原子上。
    DOI:
    10.1002/anie.201412468
  • 作为产物:
    描述:
    7-(tetrahydro-2H-pyran-2-yloxy)hept-2-yn-1-ol4-甲基苯磺酸吡啶 作用下, 以 乙醇 为溶剂, 反应 5.0h, 以76%的产率得到hept-2-yne-1,7-diol
    参考文献:
    名称:
    Branched-chain and unsaturated 1,7-Diaminoheptane derivatives as deoxyhypusine synthase inhibitors
    摘要:
    Deoxyhypusine synthase catalyzes the first step in the posttranslational biosynthesis of the unusual amino acid hypusine [N-epsilon-(4-amino-2-hydroxybutyl)lysine] in eukaryotic translation initiation factor 5A (eIF-SA). eIF-SA and its single hypusine residue are essential for cell proliferation. Two series of 1,7-diaminoheptane derivatives were prepared and tested as inhibitors of human deoxyhypusine synthase. These include branched-chain saturated derivatives and both branched- and straight-chain unsaturated derivatives providing size and positional variation in branching and different torsional constraints. Of the branched-chain compounds, 7-amino-1-guanidinooctane (39) proved to be the most potent inhibitor in vitro (IC50, 34 nM), while 1,7-diamino-trans-hept-3-ene (20a) displayed the greatest inhibition (IC50, 0.7 mu M) among the unsaturated compounds. Compound 39 also provided effective inhibition of hypusine production in Chinese hamster ovary cells in culture. Considerations of the in vitro inhibition data reported here, along with earlier findings, allowed some speculation concerning the conformation of the substrate spermidine during its productive interaction at the active site of deoxyhypusine synthase. Published by Elsevier Science Ltd.
    DOI:
    10.1016/s0968-0896(97)10030-x
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文献信息

  • Hydrogenation Promoter, Hydrogenation Catalyst, and Process for Producing Alkene Compound
    申请人:Hori Junichi
    公开号:US20080033221A1
    公开(公告)日:2008-02-07
    A hydrogenation promoter of the present invention is produced by reacting an alkyne compound or an alkene compound, a palladium compound represented by a general formula Pd(II)X j L k (where L represents a monodentate ligand or a polydendate ligand other than a phosphorus-containing ligand (when two or more Ls are present in the compound, the Ls may be the same or different), X represents an anionic group, j represents a value determined according to the valence of X so that X j has a valence of −2 as a whole, and k represents an integer in the range of 0 to 4), and a base in an organic solvent. Specifically, The hydrogenation promoter of the invention includes palladium nanoparticles containing the alkyne compound or the alkene compound as an agglomeration-preventing agent.
    本发明的氢化促进剂是通过在有机溶剂中反应炔烃化合物或烯烃化合物、由一般式Pd(II)XjLk表示的化合物(其中L表示单齿配体或不含的多齿配体(当化合物中存在两个或两个以上的L时,L可以相同也可以不同),X表示阴离子基团,j表示根据X的价确定的值,使Xj整体价为-2,k表示0到4之间的整数),以及碱的反应产生的。具体来说,本发明的氢化促进剂包括含有炔烃化合物或烯烃化合物作为凝聚抑制剂纳米粒子。
  • Crombie et al., Journal of the Chemical Society, 1956, p. 136,141
    作者:Crombie et al.
    DOI:——
    日期:——
  • New ferracyclic π-allyl and η3-pentadienyl complexes by carbonylative lactonization of unsaturated diols
    作者:Rainer Schobert、Hermann Pfab、Anett Mangold、Frank Hampel
    DOI:10.1016/s0020-1693(99)00041-9
    日期:1999.8
    Various types of mono- and binuclear ferracyclic (eta(3)-allyl)iron complexes were prepared from unsaturated diols. Chelated tricarbonylironcarbene complexes 5 and 7 featuring a partially ligated (1,3-eta(3))-pentadienyl ligand were built up from the diene-1,2-diols 4 or 8, respectively. 2-Hexyn-4-ene-1,6-diol (12) reacted with enneacarbonyldiiron to furnish the binuclear 1-lactonyl-(1,3-pi:2-sigma)-allyldiiron complex 13 under mild conditions. Its structural details are discussed. Similar complexes 17 with five- to seven-membered lactone substituents at the allyl ligand were prepared likewise from the corresponding 2-alkyne-1,n-diols (16). (C) 1999 Elsevier Science S.A. All rights reserved.
  • US7619125B2
    申请人:——
    公开号:US7619125B2
    公开(公告)日:2009-11-17
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