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3-[2-(3-Hydroxy-propoxy)-1-(3-hydroxy-propoxymethyl)-ethoxy]-propan-1-ol | 16607-62-8

中文名称
——
中文别名
——
英文名称
3-[2-(3-Hydroxy-propoxy)-1-(3-hydroxy-propoxymethyl)-ethoxy]-propan-1-ol
英文别名
1-Propanol, 3,3',3''-[1,2,3-propanetriyltris(oxy)]tris-;3-[2,3-bis(3-hydroxypropoxy)propoxy]propan-1-ol
3-[2-(3-Hydroxy-propoxy)-1-(3-hydroxy-propoxymethyl)-ethoxy]-propan-1-ol化学式
CAS
16607-62-8
化学式
C12H26O6
mdl
——
分子量
266.335
InChiKey
DMABVNLMIWMRNK-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):
    -1.1
  • 重原子数:
    18
  • 可旋转键数:
    14
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    88.4
  • 氢给体数:
    3
  • 氢受体数:
    6

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

反应信息

  • 作为反应物:
    描述:
    3-[2-(3-Hydroxy-propoxy)-1-(3-hydroxy-propoxymethyl)-ethoxy]-propan-1-ol 在 9-borabicyclo[3.3.1]nonane dimer 、 sodium hydride 作用下, 以 四氢呋喃N,N-二甲基甲酰胺 为溶剂, 反应 4.0h, 生成 1,2,3-tris-O-[2-(2-hydroxyethoxy)ethyl]glycerol
    参考文献:
    名称:
    Synthesis of divalent β-(1→6)-branched (1→3)-glucohexaose and trivalent β-(1→6)-branched (1→3)-glucotriose
    摘要:
    Hexaose, beta-D-Glcp-(1-->3)-[beta-D-Glcp-(1-->6)]-alpha-D-Glcp-(1-->3)-beta-D-Glcp-(1-->3)-[beta-D-Glcp-(1-->6)]-beta-D-Glcp, based dirners were synthesized by twofold glycosidation of the hexaosyl trichloroacetimidate with hexylene 1,6-diol, diethylene glycol and triethylene glycol, respectively. Meanwhile, a triose, beta-1D-Glcp-(1-->3)-[betaD-Glcp-(1-->6)]-beta-D-Glcp,based trimer was obtained by glycosidation of the triosyl trichloroacetimidate with a glycerol-derived triol scaffold. (C) 2004 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.carres.2004.09.016
  • 作为产物:
    描述:
    3-[2,3-二(丙-2-烯氧基)丙氧基]丙-1-烯 在 9-borabicyclo[3.3.1]nonane dimer 、 sodium hydroxide双氧水 作用下, 以 四氢呋喃 为溶剂, 反应 2.0h, 生成 3-[2-(3-Hydroxy-propoxy)-1-(3-hydroxy-propoxymethyl)-ethoxy]-propan-1-ol
    参考文献:
    名称:
    Synthesis of divalent β-(1→6)-branched (1→3)-glucohexaose and trivalent β-(1→6)-branched (1→3)-glucotriose
    摘要:
    Hexaose, beta-D-Glcp-(1-->3)-[beta-D-Glcp-(1-->6)]-alpha-D-Glcp-(1-->3)-beta-D-Glcp-(1-->3)-[beta-D-Glcp-(1-->6)]-beta-D-Glcp, based dirners were synthesized by twofold glycosidation of the hexaosyl trichloroacetimidate with hexylene 1,6-diol, diethylene glycol and triethylene glycol, respectively. Meanwhile, a triose, beta-1D-Glcp-(1-->3)-[betaD-Glcp-(1-->6)]-beta-D-Glcp,based trimer was obtained by glycosidation of the triosyl trichloroacetimidate with a glycerol-derived triol scaffold. (C) 2004 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.carres.2004.09.016
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文献信息

  • Ink Carriers Containing Low Viscosity Functionalized Waxes, Phase Change Inks Including Same, And Methods For Making Same
    申请人:Goredema Adela
    公开号:US20100075038A1
    公开(公告)日:2010-03-25
    A phase change ink including a colorant and a carrier including a tri-ester of the formula wherein R 1 , R 2 and R 3 , and n are as defined herein.
  • CURABLE COMPOSITION AND IMAGE FORMING METHOD
    申请人:FUJIFILM CORPORATION
    公开号:US20150210876A1
    公开(公告)日:2015-07-30
    A curable composition includes a polyfunctional polymerizable compound A1 represented by the following general formula (1) and a polyfunctional compound A2 which differs from A1. (In the formula, R 1 represents a hydrogen atom or a methyl group. L 1 represents a linear or branched alkylene group having 2 to 4 carbon atoms. However, L 1 does not have a structure in which the oxygen atom and the nitrogen atom bonded on both ends of L 1 are bonded to the same carbon atom of L 1 . L 2 represents a divalent linking group. k represents 2 or 3. x, y, and z each independently represent integers of 0 to 6, and x+y+z equals 0 to 18.)
  • US3997702A
    申请人:——
    公开号:US3997702A
    公开(公告)日:1976-12-14
  • US5233006A
    申请人:——
    公开号:US5233006A
    公开(公告)日:1993-08-03
  • US5399738A
    申请人:——
    公开号:US5399738A
    公开(公告)日:1995-03-21
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