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Chlor-dimethylamino-trifluormethyl-phosphin | 3135-63-5

中文名称
——
中文别名
——
英文名称
Chlor-dimethylamino-trifluormethyl-phosphin
英文别名
Trifluormethyl-dimethylamino-chlorphosphin;Chlor--trifluormethyl-phosphin;Phosphonamidous chloride, N,N-dimethyl-P-(trifluoromethyl)-;N-[chloro(trifluoromethyl)phosphanyl]-N-methylmethanamine
Chlor-dimethylamino-trifluormethyl-phosphin化学式
CAS
3135-63-5
化学式
C3H6ClF3NP
mdl
——
分子量
179.509
InChiKey
WTKYQWKIVWZVJF-UHFFFAOYSA-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:
    83.6±45.0 °C(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    2.2
  • 重原子数:
    9
  • 可旋转键数:
    1
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    3.2
  • 氢给体数:
    0
  • 氢受体数:
    4

SDS

SDS:9cc0ae18910034b82db90604aa9e29ed
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反应信息

  • 作为反应物:
    描述:
    Chlor-dimethylamino-trifluormethyl-phosphin保护胸苷三乙胺 作用下, 以 二氯甲烷 为溶剂, 反应 12.0h, 生成
    参考文献:
    名称:
    Studies on trifluoromethylphosphonamidite analogues as building blocks in oligonucleotide synthesis
    摘要:
    The phosphorylating reagents CF3P(NMe(2))Cl and CF3P(NEt(2))Cl are used to phosphorylate the 3'-hydroxyl moiety of several protected 2'-deoxynucleosides yielding the corresponding nucleoside trifluoromethyl phosphonamidites. Their scope and limitations towards amidite activation are investigated but, however, their behavior is completely different to commonly used nucleoside phosphorus amidites.
    DOI:
    10.1016/0040-4039(95)00186-g
  • 作为产物:
    描述:
    Bis---phosphin盐酸 作用下, 以 乙醚 为溶剂, 生成 Chlor-dimethylamino-trifluormethyl-phosphin
    参考文献:
    名称:
    Studies on trifluoromethylphosphonamidite analogues as building blocks in oligonucleotide synthesis
    摘要:
    The phosphorylating reagents CF3P(NMe(2))Cl and CF3P(NEt(2))Cl are used to phosphorylate the 3'-hydroxyl moiety of several protected 2'-deoxynucleosides yielding the corresponding nucleoside trifluoromethyl phosphonamidites. Their scope and limitations towards amidite activation are investigated but, however, their behavior is completely different to commonly used nucleoside phosphorus amidites.
    DOI:
    10.1016/0040-4039(95)00186-g
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文献信息

  • Gmelin Handbuch der Anorganischen Chemie, Gmelin Handbook: F: PerFHalOrg.3, 1.9, page 70 - 123
    作者:
    DOI:——
    日期:——
  • Nixon, J. F.; Cavell, R. G., Journal of the Chemical Society
    作者:Nixon, J. F.、Cavell, R. G.
    DOI:——
    日期:——
  • Phosphines Containing the CH<sub>3</sub>CF<sub>3</sub>P Group<sup>1</sup>
    作者:Anton B. Burg、K. K. Joshi、John F. Nixon
    DOI:10.1021/ja00953a007
    日期:1966.1
  • Studies on trifluoromethylphosphonamidite analogues as building blocks in oligonucleotide synthesis
    作者:Michael Mayer、Ivar Ugi、Wolfgang Richter
    DOI:10.1016/0040-4039(95)00186-g
    日期:1995.3
    The phosphorylating reagents CF3P(NMe(2))Cl and CF3P(NEt(2))Cl are used to phosphorylate the 3'-hydroxyl moiety of several protected 2'-deoxynucleosides yielding the corresponding nucleoside trifluoromethyl phosphonamidites. Their scope and limitations towards amidite activation are investigated but, however, their behavior is completely different to commonly used nucleoside phosphorus amidites.
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