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61,63-Di-O-trityl-cG7 permethylate | 139622-72-3

中文名称
——
中文别名
——
英文名称
61,63-Di-O-trityl-cG7 permethylate
英文别名
61,63-Di-O-trityl-cG7 permethylate
61,63-Di-O-trityl-cG7 permethylate化学式
CAS
139622-72-3
化学式
C99H136O35
mdl
——
分子量
1886.15
InChiKey
NCJICKCMAQHLPE-RXMSSMPFSA-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):
    7.23
  • 重原子数:
    134.0
  • 可旋转键数:
    36.0
  • 环数:
    27.0
  • sp3杂化的碳原子比例:
    0.64
  • 拓扑面积:
    323.05
  • 氢给体数:
    0.0
  • 氢受体数:
    35.0

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:
    参考文献:
    名称:
    Preparation of di-O-triphenylmethyl-(trityl)-cyclomalto-hexaoses and -cyclomaltoheptaoses and characterization of three positional isomers of each by the “hex-5-enose degradation”
    摘要:
    Regioisomeric 6l,6n-di-O-trityl-cyclomaltohexaoses (cG6s) or -cyclomaltoheptaoses (cG7s) were prepared by the reaction of cyclomaltohexaose (1, cG6) or cylomaltoheptaose (5, cG7) with chlorotriphenylmethane methane in pyridine and isolation by h.p.l.c. The regiochemical determination of each three ditrityl-substituted substituted derivatives has been accomplished by the "hex-5-enose degradation", followed by measurement of their f.a.b.-mass spectra.
    DOI:
    10.1016/0008-6215(92)80001-h
  • 作为产物:
    描述:
    61,63-Di-O-tritylcyclomaltoheptaose碘甲烷 在 sodium hydride 作用下, 以 N,N-二甲基甲酰胺 为溶剂, 反应 5.0h, 以61.2%的产率得到61,63-Di-O-trityl-cG7 permethylate
    参考文献:
    名称:
    Preparation of di-O-triphenylmethyl-(trityl)-cyclomalto-hexaoses and -cyclomaltoheptaoses and characterization of three positional isomers of each by the “hex-5-enose degradation”
    摘要:
    Regioisomeric 6l,6n-di-O-trityl-cyclomaltohexaoses (cG6s) or -cyclomaltoheptaoses (cG7s) were prepared by the reaction of cyclomaltohexaose (1, cG6) or cylomaltoheptaose (5, cG7) with chlorotriphenylmethane methane in pyridine and isolation by h.p.l.c. The regiochemical determination of each three ditrityl-substituted substituted derivatives has been accomplished by the "hex-5-enose degradation", followed by measurement of their f.a.b.-mass spectra.
    DOI:
    10.1016/0008-6215(92)80001-h
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