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| 1350321-41-3

中文名称
——
中文别名
——
英文名称
——
英文别名
——
化学式
CAS
1350321-41-3
化学式
C7H12N6O2
mdl
——
分子量
212.211
InChiKey
HZMITQGKJBCWCV-BNHYGAARSA-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):
    1.51
  • 重原子数:
    15.0
  • 可旋转键数:
    3.0
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    126.98
  • 氢给体数:
    1.0
  • 氢受体数:
    4.0

反应信息

  • 作为反应物:
    描述:
    偶氮二甲酸二异丙酯叠氮磷酸二苯酯 、 palladium 10% on activated carbon 、 palladium on carbon 、 氢气potassium carbonate三乙胺三苯基膦 作用下, 以 四氢呋喃甲醇 为溶剂, 反应 29.5h, 生成 di-tert-butyl ((1R,3S,4S,6R)-4-amino-6-methoxycyclohexane-1,3-diyl)dicarbamate
    参考文献:
    名称:
    Conjugate of neamine and 2-deoxystreptamine mimic connected by an amide bond
    摘要:
    An amino-functionalized 2-deoxystreptamine (2-DOS) mimic was conjugated by an amide bond to a neamine moiety containing a carboxylic acid in ring II. A library of A-site RNA and its mutants was prepared to examine RNA binding characteristics of the additional 2-DOS moiety attached to neamine. The 2-DOS mimic conjugated to the neamine increased binding affinity up to 200-folds compared to that of neamine. The conjugate binds to native A-site RNA and its mutants with up to 6-fold difference in sequence selectivity. (C) 2011 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2011.06.084
  • 作为产物:
    描述:
    盐酸 作用下, 以 甲醇 为溶剂, 反应 1.0h, 以97%的产率得到
    参考文献:
    名称:
    Conjugate of neamine and 2-deoxystreptamine mimic connected by an amide bond
    摘要:
    An amino-functionalized 2-deoxystreptamine (2-DOS) mimic was conjugated by an amide bond to a neamine moiety containing a carboxylic acid in ring II. A library of A-site RNA and its mutants was prepared to examine RNA binding characteristics of the additional 2-DOS moiety attached to neamine. The 2-DOS mimic conjugated to the neamine increased binding affinity up to 200-folds compared to that of neamine. The conjugate binds to native A-site RNA and its mutants with up to 6-fold difference in sequence selectivity. (C) 2011 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2011.06.084
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