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(S)-4-(2-[1,3,2]Dithiaphospholan-2-yl-ethyl)-2,2-dimethyl-[1,3]dioxolane | 1026352-42-0

中文名称
——
中文别名
——
英文名称
(S)-4-(2-[1,3,2]Dithiaphospholan-2-yl-ethyl)-2,2-dimethyl-[1,3]dioxolane
英文别名
(4S)-4-[2-(1,3,2-dithiaphospholan-2-yl)ethyl]-2,2-dimethyl-1,3-dioxolane
(S)-4-(2-[1,3,2]Dithiaphospholan-2-yl-ethyl)-2,2-dimethyl-[1,3]dioxolane化学式
CAS
1026352-42-0
化学式
C9H17O2PS2
mdl
——
分子量
252.339
InChiKey
SVVWLFGKGYJGKD-QMMMGPOBSA-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):
    1.2
  • 重原子数:
    14
  • 可旋转键数:
    3
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    69.1
  • 氢给体数:
    0
  • 氢受体数:
    4

反应信息

  • 作为反应物:
    描述:
    (S)-4-(2-[1,3,2]Dithiaphospholan-2-yl-ethyl)-2,2-dimethyl-[1,3]dioxolane1,2,3,4,5,6,7,8-八硫杂环辛烷1,8-二氮杂双环[5.4.0]十一碳-7-烯 作用下, 以 乙腈 为溶剂, 反应 1.0h, 生成 2-[2-[(4S)-2,2-dimethyl-1,3-dioxolan-4-yl]ethyl-sulfidophosphinothioyl]oxyethyl-trimethylazanium
    参考文献:
    名称:
    General Route to Phosphonodithioic Acid Derivatives
    摘要:
    A general procedure for the synthesis of esters of phosphonodithioic acids has been developed. The method involves the reaction of the Grignard reagents 2a-h with 2-chloro-1,3,2-dithiaphospholane (1) to give 3a-h that were sulfurized using elemental sulfur to furnish the intermediate phosphonotrithioates 4a-h, reaction of which with a variety of alcohols in the presence of DBU furnished the desired phosphonodithioates 5a-h and 6-9.
    DOI:
    10.1021/jo00105a007
  • 作为产物:
    描述:
    2-Chloro-1,3,2-dithiaphospholane 、 alkaline earth salt of/the/ methylsulfuric acid 以 四氢呋喃 为溶剂, 反应 1.0h, 生成 (S)-4-(2-[1,3,2]Dithiaphospholan-2-yl-ethyl)-2,2-dimethyl-[1,3]dioxolane
    参考文献:
    名称:
    General Route to Phosphonodithioic Acid Derivatives
    摘要:
    A general procedure for the synthesis of esters of phosphonodithioic acids has been developed. The method involves the reaction of the Grignard reagents 2a-h with 2-chloro-1,3,2-dithiaphospholane (1) to give 3a-h that were sulfurized using elemental sulfur to furnish the intermediate phosphonotrithioates 4a-h, reaction of which with a variety of alcohols in the presence of DBU furnished the desired phosphonodithioates 5a-h and 6-9.
    DOI:
    10.1021/jo00105a007
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文献信息

  • General Route to Phosphonodithioic Acid Derivatives
    作者:Stephen F. Martin、Allan S. Wagman、G. Greg Zipp、Mikhail K. Gratchev
    DOI:10.1021/jo00105a007
    日期:1994.12
    A general procedure for the synthesis of esters of phosphonodithioic acids has been developed. The method involves the reaction of the Grignard reagents 2a-h with 2-chloro-1,3,2-dithiaphospholane (1) to give 3a-h that were sulfurized using elemental sulfur to furnish the intermediate phosphonotrithioates 4a-h, reaction of which with a variety of alcohols in the presence of DBU furnished the desired phosphonodithioates 5a-h and 6-9.
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