摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

bis(D-galacto-2,3,4,5,6-pentahydroxyhexyl)amine | 106565-39-3

中文名称
——
中文别名
——
英文名称
bis(D-galacto-2,3,4,5,6-pentahydroxyhexyl)amine
英文别名
1,1'-imino-bis-(D-1-deoxy-galactitol);Bis-(Dr-2cF,4tF,5rF,6-pentahydroxy-hexyl)-amin;1,1'-Imino-bis-(D-1-desoxy-galactit);Di-D-galactit-1-yl-amin;Di-D-galaktityl-(1)-amin;(2R,3S,4R,5S)-6-[[(2S,3R,4S,5R)-2,3,4,5,6-pentahydroxyhexyl]amino]hexane-1,2,3,4,5-pentol
bis(D-galacto-2,3,4,5,6-pentahydroxyhexyl)amine化学式
CAS
106565-39-3
化学式
C12H27NO10
mdl
——
分子量
345.347
InChiKey
KXONZRPGKNOGCG-NKUXFBMISA-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:
    785.5±60.0 °C(Predicted)
  • 密度:
    1.617±0.06 g/cm3(Temp: 20 °C; Press: 760 Torr)(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    -6
  • 重原子数:
    23
  • 可旋转键数:
    12
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    214
  • 氢给体数:
    11
  • 氢受体数:
    11

反应信息

  • 作为反应物:
    描述:
    bis(D-galacto-2,3,4,5,6-pentahydroxyhexyl)amine乙酸酐 为溶剂, 生成 N-Acetyl-di-D-galaktityl-(1)-amin
    参考文献:
    名称:
    Preparation and Properties of Dialditylamines1
    摘要:
    DOI:
    10.1021/jo01045a071
  • 作为产物:
    描述:
    galactose oxime 在 platinum on activated charcoal 氢气 作用下, 以 为溶剂, 50.0 ℃ 、10.13 MPa 条件下, 反应 24.0h, 以79.5%的产率得到bis(D-galacto-2,3,4,5,6-pentahydroxyhexyl)amine
    参考文献:
    名称:
    Formation of borate esters from, and sequestration of metal ions by, bis(polyhydroxyalkyl)amines and their N-carboxymethyl derivatives studied by 11B and 13C NMR spectroscopy
    摘要:
    Catalytic hydrogenation of aldose oximes affords bis(polyhydroxyalkyl)amines. These compounds and their N-carboxymethyl derivatives react with borate ions to give macrocyclic diborate diesters. The presence of an N-carboxymethyl group raises the capacities for the sequestration of Ca2+, Cu2+, and Cd2+. The N-carboxymethyl derivatives possess strong affinity for Ca2+ (pH > 11) and Cd2+ both in the absence and presence of borate.
    DOI:
    10.1016/0008-6215(93)87032-n
点击查看最新优质反应信息

文献信息

  • The Preparation of Glycamines<sup>1</sup>
    作者:Fred Kagan、M. A. Rebenstorf、Richard V. Heinzelman
    DOI:10.1021/ja01570a063
    日期:1957.7
  • Synthesis of Amino Compounds in the Sugar Series by Phenylhydrazone Reduction<sup>1,2</sup>
    作者:M. L. WOLFROM、F. SHAFIZADEH、J. O. WEHRMÜLLER、R. K. ARMSTRONG
    DOI:10.1021/jo01098a019
    日期:1958.4
  • Preparation and Properties of Dialditylamines<sup>1</sup>
    作者:J. E. Hodge、B. F. Moy
    DOI:10.1021/jo01045a071
    日期:1963.10
  • Formation of borate esters from, and sequestration of metal ions by, bis(polyhydroxyalkyl)amines and their N-carboxymethyl derivatives studied by 11B and 13C NMR spectroscopy
    作者:Jacco van Haveren、Hendrik Lammers、Joop A. Peters、Jan G. Batelaan、Herman van Bekkum
    DOI:10.1016/0008-6215(93)87032-n
    日期:1993.5
    Catalytic hydrogenation of aldose oximes affords bis(polyhydroxyalkyl)amines. These compounds and their N-carboxymethyl derivatives react with borate ions to give macrocyclic diborate diesters. The presence of an N-carboxymethyl group raises the capacities for the sequestration of Ca2+, Cu2+, and Cd2+. The N-carboxymethyl derivatives possess strong affinity for Ca2+ (pH > 11) and Cd2+ both in the absence and presence of borate.
查看更多