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Mono-2-O-(4-azidobutyl)-β-cyclodextrin

中文名称
——
中文别名
——
英文名称
Mono-2-O-(4-azidobutyl)-β-cyclodextrin
英文别名
(1S,3R,5R,6S,8R,10R,11S,13R,15R,16S,18R,20R,21S,23R,25R,26S,28R,30R,31S,33R,35R,36R,37R,38R,39R,40R,41R,42R,43R,44R,45R,46S,47R,48R,49R)-47-(4-azidobutoxy)-5,10,15,20,25,30,35-heptakis(hydroxymethyl)-2,4,7,9,12,14,17,19,22,24,27,29,32,34-tetradecaoxaoctacyclo[31.2.2.23,6.28,11.213,16.218,21.223,26.228,31]nonatetracontane-36,37,38,39,40,41,42,43,44,45,46,48,49-tridecol
Mono-2-O-(4-azidobutyl)-β-cyclodextrin化学式
CAS
——
化学式
C46H77N3O35
mdl
——
分子量
1232.12
InChiKey
AJHLXVNZZDWDLG-VMRFEQBZSA-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):
    -12.9
  • 重原子数:
    84
  • 可旋转键数:
    13
  • 环数:
    21.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    557
  • 氢给体数:
    20
  • 氢受体数:
    37

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:
    Mono-2-O-(4-azidobutyl)-β-cyclodextrinammonium hydroxide三苯基膦 作用下, 生成 Mono-2-O-(4-aminobutyl)-β-cyclodextrin
    参考文献:
    名称:
    The Synthesis of Functionalized Cyclodextrins As Scaffolds and Templates for Molecular Diversity, Catalysis, and Inclusion Phenomena
    摘要:
    alpha-, beta- and gamma-cyclodextrins were chemically modified to selectively introduce functionality on the primary and secondary faces. Azido and substituted alkenyl groups were selectively introduced on the primary hydroxy groups to give monosubstituted derivatives. The secondary C-2 hydroxy group was selectively functionalized with allyl, 1-hexenyl, carboxymethyl, and omega-azidoalkyl groups (n: 3, 4, 5) as ethers. The chemically modified cyclodextrins are versatile molecules for use as scaffolds and templates in conjunction with chemical diversity, catalysis, and inclusion phenomena.
    DOI:
    10.1021/jo00120a023
  • 作为产物:
    描述:
    1-azido-4-iodobutaneβ-环糊精 在 lithium hydride 作用下, 以 二甲基亚砜 为溶剂, 以25%的产率得到Mono-2-O-(4-azidobutyl)-β-cyclodextrin
    参考文献:
    名称:
    The Synthesis of Functionalized Cyclodextrins As Scaffolds and Templates for Molecular Diversity, Catalysis, and Inclusion Phenomena
    摘要:
    alpha-, beta- and gamma-cyclodextrins were chemically modified to selectively introduce functionality on the primary and secondary faces. Azido and substituted alkenyl groups were selectively introduced on the primary hydroxy groups to give monosubstituted derivatives. The secondary C-2 hydroxy group was selectively functionalized with allyl, 1-hexenyl, carboxymethyl, and omega-azidoalkyl groups (n: 3, 4, 5) as ethers. The chemically modified cyclodextrins are versatile molecules for use as scaffolds and templates in conjunction with chemical diversity, catalysis, and inclusion phenomena.
    DOI:
    10.1021/jo00120a023
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文献信息

  • The Synthesis of Functionalized Cyclodextrins As Scaffolds and Templates for Molecular Diversity, Catalysis, and Inclusion Phenomena
    作者:Stephen Hanessian、Aziza Benalil、Craig Laferriere
    DOI:10.1021/jo00120a023
    日期:1995.7
    alpha-, beta- and gamma-cyclodextrins were chemically modified to selectively introduce functionality on the primary and secondary faces. Azido and substituted alkenyl groups were selectively introduced on the primary hydroxy groups to give monosubstituted derivatives. The secondary C-2 hydroxy group was selectively functionalized with allyl, 1-hexenyl, carboxymethyl, and omega-azidoalkyl groups (n: 3, 4, 5) as ethers. The chemically modified cyclodextrins are versatile molecules for use as scaffolds and templates in conjunction with chemical diversity, catalysis, and inclusion phenomena.
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