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12,14-dioxa-13-phosphapentacyclo[13.8.0.02,11.03,8.018,23]tricosa-1(15),2(11),3,5,7,9,16,18,20,22-decaen-13-yloxy(triphenyl)silane | 150646-49-4

中文名称
——
中文别名
——
英文名称
12,14-dioxa-13-phosphapentacyclo[13.8.0.02,11.03,8.018,23]tricosa-1(15),2(11),3,5,7,9,16,18,20,22-decaen-13-yloxy(triphenyl)silane
英文别名
——
12,14-dioxa-13-phosphapentacyclo[13.8.0.02,11.03,8.018,23]tricosa-1(15),2(11),3,5,7,9,16,18,20,22-decaen-13-yloxy(triphenyl)silane化学式
CAS
150646-49-4
化学式
C38H27O3PSi
mdl
——
分子量
590.69
InChiKey
WUDVPTPBCGKRAU-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:
    690.8±28.0 °C(predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    8.69
  • 重原子数:
    43.0
  • 可旋转键数:
    5.0
  • 环数:
    8.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    35.51
  • 氢给体数:
    0.0
  • 氢受体数:
    3.0

反应信息

  • 作为反应物:
    描述:
    苯甲醛12,14-dioxa-13-phosphapentacyclo[13.8.0.02,11.03,8.018,23]tricosa-1(15),2(11),3,5,7,9,16,18,20,22-decaen-13-yloxy(triphenyl)silane甲苯 为溶剂, 反应 72.0h, 以11%的产率得到[(13-oxo-12,14-dioxa-13λ5-phosphapentacyclo[13.8.0.02,11.03,8.018,23]tricosa-1(15),2(11),3,5,7,9,16,18,20,22-decaen-13-yl)-phenylmethoxy]-triphenylsilane
    参考文献:
    名称:
    Asymmetric Silylphosphite Esters: Synthesis and Reactivity of (rac-O,O-Binaphtholato)POSiR3(R3= Ph3,tBuMe2, Et3)
    摘要:
    The new, silylphosphite compounds, (rac-O,O-binaphtholato)POSiR3 (R3 = Ph3, tBuMe2, Et3) have been synthesised by the reactions of (rac-O,O-binaphtholato)PCl and R3SiOH. The abilities of these silylphosphite esters to act as phosphonylating agents towards benzaldehyde have been investigated.
    DOI:
    10.1080/00397919308011262
  • 作为产物:
    参考文献:
    名称:
    Asymmetric Silylphosphite Esters: Synthesis and Reactivity of (rac-O,O-Binaphtholato)POSiR3(R3= Ph3,tBuMe2, Et3)
    摘要:
    The new, silylphosphite compounds, (rac-O,O-binaphtholato)POSiR3 (R3 = Ph3, tBuMe2, Et3) have been synthesised by the reactions of (rac-O,O-binaphtholato)PCl and R3SiOH. The abilities of these silylphosphite esters to act as phosphonylating agents towards benzaldehyde have been investigated.
    DOI:
    10.1080/00397919308011262
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