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1,4-anhydro-D-allitol | 51607-77-3

中文名称
——
中文别名
——
英文名称
1,4-anhydro-D-allitol
英文别名
1,4-Anhydro-D-altritol;1,4-Anhydro-D-allit;(2R,3S,4S)-2-[(1R)-1,2-dihydroxyethyl]oxolane-3,4-diol
1,4-anhydro-D-allitol化学式
CAS
51607-77-3
化学式
C6H12O5
mdl
——
分子量
164.158
InChiKey
JNYAEWCLZODPBN-DPYQTVNSSA-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

物化性质

  • 沸点:
    442.5±40.0 °C(Predicted)
  • 密度:
    1.573±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    -2.1
  • 重原子数:
    11
  • 可旋转键数:
    2
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    90.2
  • 氢给体数:
    4
  • 氢受体数:
    5

文献信息

  • Phenol-Free Overbased Alkaline Earth Metal Carboxylate
    申请人:Ferro Corporation
    公开号:US20160017118A1
    公开(公告)日:2016-01-21
    A phenol-free overbased alkaline earth metal carboxylate is obtained by reacting a cyclic ether alcohol, an alkaline earth metal hydroxide, a fatty carboxylic acid, carbon dioxide, an optional fatty alcohol, and an optional liquid hydrocarbon solvent or oil.
  • PHOSPHONIC ACID CATALYST IN DEHYDRATIVE CYCLIZATION OF 5 AND 6 CARBON POLYOLS WITH IMPROVED COLOR AND PRODUCT ACCOUNTABILITY
    申请人:ARCHER DANIELS MIDLAND COMPANY
    公开号:US20170015676A1
    公开(公告)日:2017-01-19
    A process for preparing materials derived from sugar alcohols such that the dehydration products exhibit better accountability and improved color to water-clear or near water-white appearance is described. In particular, the process involves employing a reducing Brønsted acid (e.g., phosphonic acid) for the catalysis of sugar alcohols to their corresponding dehydrated-cyclized products.
  • US9382403B2
    申请人:——
    公开号:US9382403B2
    公开(公告)日:2016-07-05
  • US9969704B2
    申请人:——
    公开号:US9969704B2
    公开(公告)日:2018-05-15
  • [EN] PHENOL-FREE OVERBASED ALKALINE EARTH METAL CARBOXYLATE<br/>[FR] CARBOXYLATE DE MÉTAL ALCALINO-TERREUX SURBASÉ EXEMPT DE PHÉNOL
    申请人:POLYMER ADDITIVES INC
    公开号:WO2016010986A1
    公开(公告)日:2016-01-21
    A phenol-free overbased alkaline earth metal carboxylate is obtained by reacting a cyclic ether alcohol, an alkaline earth metal hydroxide, a fatty carboxylic acid, carbon dioxide, an optional fatty alcohol, and an optional liquid hydrocarbon solvent or oil.
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