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(2S,3S,4R,5R)-2,6-Dimethoxy-hexane-1,3,4,5-tetraol | 20316-54-5

中文名称
——
中文别名
——
英文名称
(2S,3S,4R,5R)-2,6-Dimethoxy-hexane-1,3,4,5-tetraol
英文别名
2,6-di-O-methyl glucitol;(2S,3S,4R,5R)-2,6-dimethoxyhexane-1,3,4,5-tetrol
(2S,3S,4R,5R)-2,6-Dimethoxy-hexane-1,3,4,5-tetraol化学式
CAS
20316-54-5
化学式
C8H18O6
mdl
——
分子量
210.227
InChiKey
CVNUXTCURWAGHC-ULAWRXDQSA-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):
    -2.5
  • 重原子数:
    14
  • 可旋转键数:
    7
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    99.4
  • 氢给体数:
    4
  • 氢受体数:
    6

反应信息

  • 作为反应物:
    描述:
    乙酸酐(2S,3S,4R,5R)-2,6-Dimethoxy-hexane-1,3,4,5-tetraol吡啶 作用下, 生成 1,3,4,5-tetra-O-acetyl-2,6-di-O-methylglucitol
    参考文献:
    名称:
    The formation of inter-residue, hemiacetal bonds during the oxidation of methyl β-lactoside
    摘要:
    DOI:
    10.1016/s0008-6215(00)85546-9
  • 作为产物:
    描述:
    methyl 2,6-di-O-methyl-3,4-di-O-(N-phenylcarbamoyl)-α-D-glucopyranoside 在 barium dihydroxide 、 sodium tetrahydroborate 、 甲酸硫酸 作用下, 反应 18.0h, 生成 (2S,3S,4R,5R)-2,6-Dimethoxy-hexane-1,3,4,5-tetraol
    参考文献:
    名称:
    The formation of inter-residue, hemiacetal bonds during the oxidation of methyl β-lactoside
    摘要:
    DOI:
    10.1016/s0008-6215(00)85546-9
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文献信息

  • Absorbent article comprising cyclodextrin complexes
    申请人:The Procter & Gamble Company
    公开号:US10183273B2
    公开(公告)日:2019-01-22
    Absorbent articles having a cyclodextrin complex of one or more odor controlling organic compounds wherein the cyclodextrin is a substituted cyclodextrin (wherein the H atom of OH groups in positions 2, 3 and 6 is partially or entirely replaced by a substituent —R) having a substitution degree (DS) of 0.4 or more —R substituents per molecule of cyclodextrin and wherein substitution in position 2 is 20% or above, in position 6 is 20% or above and in position 3 is 50% or below. Cyclodextrin complexes of this type release the odor controlling organic compound much faster and in more complete manner than non-substituted or differently substituted cyclodextrin complexes thus the odor control efficacy is improved.
    具有一种或多种气味控制有机化合物的环糊精复合物的吸附用品,其中的环糊精是一种取代的环糊精(其中第 2、3 和 6 位上 OH 基团的 H 原子部分或全部被取代基 -R 取代),其取代度(DS)为每分子环糊精 0.4 个或更多 -R 取代基,其中第 2 位上的取代度为 20%或以上,第 6 位上的取代度为 20%或以上,第 3 位上的取代度为 50%或以下。与未取代或不同取代的环糊精复合物相比,这种类型的环糊精复合物释放气味控制有机化合物的速度更快、更彻底,从而提高了气味控制效果。
  • ABSORBENT ARTICLE COMPRISING CYCLODEXTRIN COMPLEXES
    申请人:The Procter & Gamble Company
    公开号:EP3474906B1
    公开(公告)日:2020-10-21
  • ABSORBENT ARTICLES COMPRISING ENCAPSULATING AGENTS
    申请人:The Procter & Gamble Company
    公开号:EP3474908A1
    公开(公告)日:2019-05-01
  • Absorbent Article Comprising Cyclodextrin Complexes
    申请人:The Procter & Gamble Company
    公开号:US20170368218A1
    公开(公告)日:2017-12-28
    Disclosed are absorbent articles having a cyclodextrin complex of one or more odor controlling organic compounds wherein the cyclodextrin is a substituted cyclodextrin (wherein the H atom of OH groups in positions 2, 3 and 6 is partially or entirely replaced by a substituent —R) having a substitution degree (DS) of 0.4 or more —R substituents per molecule of cyclodextrin and wherein substitution in position 2 is 20% or above, in position 6 is 20% or above and in position 3 is 50% or below. Cyclodextrin complexes of this type release the odor controlling organic compound much faster and in more complete manner than non-substituted or differently substituted cyclodextrin complexes thus the odor control efficacy is improved.
  • [EN] ABSORBENT ARTICLE COMPRISING CYCLODEXTRIN COMPLEXES<br/>[FR] ARTICLE ABSORBANT COMPRENANT DES COMPLEXES DE CYCLODEXTRINE
    申请人:PROCTER & GAMBLE
    公开号:WO2017223439A1
    公开(公告)日:2017-12-28
    Disclosed are absorbent articles having a cyclodextrin complex of one or more odor controlling organic compounds wherein the cyclodextrin is a substituted cyclodextrin (wherein the H atom of OH groups in positions 2, 3 and 6 is partially or entirely replaced by a substituent -R) having a substitution degree (DS) of 0,4 or more -R substituents per molecule of cyclodextrin and wherein substitution in position 2 is 20% or above, in position 6 is 20% or above and in position 3 is 50% or below. Cyclodextrin complexes of this type release the odor controlling organic compound much faster and in more complete manner than non-substituted or differently substituted cyclodextrin complexes thus the odor control efficacy is improved.
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