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1-hydroxy-3,6,7,7,8-pentamethyl-8-oxo-8-phospha-9-oxabicyclo<4.3.0>nonane | 104746-51-2

中文名称
——
中文别名
——
英文名称
1-hydroxy-3,6,7,7,8-pentamethyl-8-oxo-8-phospha-9-oxabicyclo<4.3.0>nonane
英文别名
2,3,3,3a,6-Pentamethyl-2-oxo-4,5,6,7-tetrahydrobenzo[d]oxaphosphol-7a-ol
1-hydroxy-3,6,7,7,8-pentamethyl-8-oxo-8-phospha-9-oxabicyclo<4.3.0>nonane化学式
CAS
104746-51-2
化学式
C12H23O3P
mdl
——
分子量
246.287
InChiKey
VQYHTRXEQJEWPM-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

计算性质

  • 辛醇/水分配系数(LogP):
    1.6
  • 重原子数:
    16
  • 可旋转键数:
    0
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    46.5
  • 氢给体数:
    1
  • 氢受体数:
    3

反应信息

  • 作为反应物:
    描述:
    重氮甲烷1-hydroxy-3,6,7,7,8-pentamethyl-8-oxo-8-phospha-9-oxabicyclo<4.3.0>nonane 生成 [1-(1,4-Dimethyl-2-oxo-cyclohexyl)-1-methyl-ethyl]-methyl-phosphinic acid methyl ester
    参考文献:
    名称:
    [1,n]二烯-IX的RPX 2 ·ALX 3合成磷杂环化合物:几种氧杂磷双环化合物的合成和结构
    摘要:
    通过在不同条件下使甲基二卤代膦与1,6-二酮和βγ-不饱和酮反应,合成了几种氧杂磷双环化合物。通过X射线衍射分析确定了一种新化合物(11)的结构。讨论了新化合物的1 H-和13 C-NMR光谱,除了11以外,还用于阐明其结构。
    DOI:
    10.1016/s0040-4020(01)96776-6
  • 作为产物:
    描述:
    甲基二氯膦methyl pulegone三氯化铝 作用下, 以 二氯甲烷 为溶剂, 反应 120.0h, 以100 mg的产率得到1-hydroxy-3,6,7,7,8-pentamethyl-8-oxo-8-phospha-9-oxabicyclo<4.3.0>nonane
    参考文献:
    名称:
    [1,n]二烯-IX的RPX 2 ·ALX 3合成磷杂环化合物:几种氧杂磷双环化合物的合成和结构
    摘要:
    通过在不同条件下使甲基二卤代膦与1,6-二酮和βγ-不饱和酮反应,合成了几种氧杂磷双环化合物。通过X射线衍射分析确定了一种新化合物(11)的结构。讨论了新化合物的1 H-和13 C-NMR光谱,除了11以外,还用于阐明其结构。
    DOI:
    10.1016/s0040-4020(01)96776-6
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文献信息

  • RUDI, A.;GOLDBERG, I.;KASHMAN, Y., TETRAHEDRON, 1985, 41, N 22, 5267-5270
    作者:RUDI, A.、GOLDBERG, I.、KASHMAN, Y.
    DOI:——
    日期:——
  • Phosphorus heterocycle synthesis by RPX2 · ALX3 addition to [1,n]dienes—IX
    作者:A. Rudi、I. Goldberg、Y. Kshman
    DOI:10.1016/s0040-4020(01)96776-6
    日期:1985.1
    Several oxaphosphabicyclic compounds were synthesized by the reaction of methyl dihalophosphane under various conditions with 1,6-diketones and βγ-unsaturated ketones. The structure of one of the new compounds (11) was established by X-ray diffraction analysis. The 1H- and 13C-NMR spectra of the new compounds, which, except for 11, served for their structure elucidation, are discussed.
    通过在不同条件下使甲基二卤代膦与1,6-二酮和βγ-不饱和酮反应,合成了几种氧杂磷双环化合物。通过X射线衍射分析确定了一种新化合物(11)的结构。讨论了新化合物的1 H-和13 C-NMR光谱,除了11以外,还用于阐明其结构。
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同类化合物

2-甲基-1,2-噁膦-5-酮 2-氧化物 3-methyl-3-trimethylsilyloxy-2-trimethylsilylamino-2-trimethylsilylimino-[1,2]-oxaphospholane 3-methyl-3-trimethylsilyloxy-2-trimethylsilylmethyl-2-trimethylsilylimino-[1,2]-oxaphospholane 3,5,5-trimethyl-3-trimethylsilyloxy-2-trimethylsilylamino-2-trimethylsilylimino-[1,2]-oxaphospholane cis-2,3,5,5-Tetramethyl-1,2-oxaphospholan-3-ol 2-oxide 2-ethyl-3,5,5-trimethyl-2-oxo-2λ5-[1,2]oxaphospholan-3-ol 2,4-Dimethyl-2-oxo-1,2-oxaphospholan 2-ethyl-5-methyl-[1,2]oxaphospholane 2-sulfide 2-Aethyl-2-oxo-1-oxa-2-phospholan 1-hydroxy-3,6,7,7,8-pentamethyl-8-oxo-8-phospha-9-oxabicyclo<4.3.0>nonane 1,2-Oxaphospholan-3-ol, 2-(ethylthio)-3,5,5-trimethyl-, 2-oxide, cis- 2,2,2-trimethyl-2λ5-[1,2]oxaphospholane 2,2,2-triethyl-2λ5-[1,2]oxaphospholane methyl 3-hydroxyl-4-terta-butyldimethylsilylbutane-1,3-cyclic thiophosphonate 2-ethyl-1,2-oxaphospholan-5-one 2-oxide 2-Methyl-2-oxo-1,2-oxaphospholan 5-Methyl-1-oxa-5λ5-phosphaspiro <4,5>-decan 5-Methyl-1-oxa-5λ5-phosphaspiro<4,4>-nonan 5-dimethylamino-7-isopropylidene-4,8,8-trimethyl-1,6-dioxa-4-aza-5λ5-phospha-spiro[4.4]nonan-9-one 2-chloromethyl-2-oxo-2λ5-[1,2]oxaphospholan-5-one 2,4-dimethyl-2-oxo-2λ5-[1,2]oxaphospholan-5-one 2-isopropylidene-3,3,3-trimethoxy-4,4-dimethyl-3λ5-[1,3]oxaphospholan-5-one 2-Oxo-1,2-oxaphospholan-2-ium 2-ethoxy-3,5,5-trimethyl-2-thioxo-2λ5-[1,2]oxaphospholan-3-ol 2,3,5,5-tetramethyl-3-chlor-1,2-oxaphospholan-2-oxide 2-tert-Butyl-3-chlor-5-methyl-1,3-oxaphospholan 1,2-oxaphospholane (3S)-2-(diethylamino)-2-hydroxy-2,3,5,5-tetramethyl-1,2lambda5-oxaphospholan-3-ol (3R)-2-(diethylamino)-2-hydroxy-2,3,5,5-tetramethyl-1,2lambda5-oxaphospholan-3-ol (2S)-2-methyl-2-oxo-1,2lambda5-oxaphospholan-5-one (2R)-2-methyl-2-oxo-1,2lambda5-oxaphospholan-5-one 2,2-bis(but-3-enoxy)-2-ethoxy-3-methyl-1,2λ5-oxaphospholane 2,2-bis(but-3-enoxy)-2,3-dimethyl-1,2λ5-oxaphospholane (5R)-5-[(1S)-1,2-dihydroxyethyl]-2-hydroxy-3-oxo-1,3-oxaphospholan-3-ium-4-one 3-(1,3-Oxaphospholan-2-yl)prop-2-enenitrile (3S)-2-ethylsulfanyl-3,5,5-trimethyl-2-oxo-1,2lambda5-oxaphospholan-3-ol 2-(Diethylamino)-3,5,5-trimethyl-2-sulfanylidene-1,2lambda5-oxaphospholan-3-ol 2-Ethyloxaphospholan-5-one (4R)-3-methyl-4-(3-methyl-1,3-oxaphospholan-4-yl)-1,3-oxaphospholane (3S)-2,3,5,5-tetramethyl-2-oxo-1,2lambda5-oxaphospholan-3-ol Diethyl-(2-thioxo-[1,2]oxaphospholan-2-yl)-amine methyl 3,4-dihydroxyl-butane-1,3-cyclic thiophosphonate 2-chloro-2-thiono-5-methyl-1,2-oxaphospholane 2-thio-2-dimethylamino-5-methyl-1,2-oxaphospholane