摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

-phenylphosphinoxyd | 29865-25-6

中文名称
——
中文别名
——
英文名称
-phenylphosphinoxyd
英文别名
(m-Chlorphenyl)-phenyl-phosphinoxid;Phenyl(m-chlorphenyl)phosphin-oxid;(m-Chlor-phenyl)-phenylphosphinoxyd
<m-Chlor-phenyl>-phenylphosphinoxyd化学式
CAS
29865-25-6
化学式
C12H10ClOP
mdl
——
分子量
236.638
InChiKey
VKWQTTSSDAXXIL-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):
    2.85
  • 重原子数:
    15.0
  • 可旋转键数:
    2.0
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    17.07
  • 氢给体数:
    0.0
  • 氢受体数:
    1.0

反应信息

  • 作为反应物:
    描述:
    1,2,3-噻唑(1,5-a)吡啶-phenylphosphinoxyd 在 copper diacetate 作用下, 以 1,4-二氧六环 为溶剂, 反应 6.0h, 以85%的产率得到(3-chlorophenyl)(phenyl)(pyridin-2-ylmethyl)phosphine oxide
    参考文献:
    名称:
    乙酸铜(II)催化的吡啶并三唑与P(O)H化合物的脱氮C-P偶联合成磷酸化的吡啶
    摘要:
    吡啶三唑与P(O)H化合物的新型廉价铜催化脱氮C-P偶联反应已得到开发。该反应通过铜催化的P(O)-H插入由吡啶三唑原位生成的吡啶基卡宾中间体的过程进行。该反应为合成各种2-picolylphosphoryl化合物提供了一种新的有效方法。
    DOI:
    10.1002/adsc.201800909
点击查看最新优质反应信息

文献信息

  • Phosphinyl Guanidine Compounds, Metal Salt Complexes, Catalyst Systems, and Their Use to Oligomerize or Polymerize Olefins
    申请人:SYDORA Orson J.
    公开号:US20130331629A1
    公开(公告)日:2013-12-12
    The present application relates to N 2 -phosphinyl guanidine metal salt complexes. The present application also relates to catalyst systems comprising N 2 -phosphinyl guanidine metal salt complexes and processes for making catalyst systems comprising N 2 -phosphinyl guanidine metal salt complexes. The present application also relates to utilizing N 2 -phosphinyl guanidine metal salt complexes in processes of oligomerizing or polymerizing olefins.
    本申请涉及N2-酰亚胺属盐配合物。本申请还涉及包含N2-酰亚胺属盐配合物的催化剂体系以及制备包含N2-酰亚胺属盐配合物的催化剂体系的方法。本申请还涉及在烯烃的齐聚或聚合过程中利用N2-酰亚胺属盐配合物。
  • Ph<sub>3</sub>P-mediated highly selective C(α)–P coupling of quinone monoacetals with R<sub>2</sub>P(O)H: convenient and practical synthesis of <i>ortho</i>-phosphinyl phenols
    作者:Ruwei Shen、Ming Zhang、Jing Xiao、Chao Dong、Li-Biao Han
    DOI:10.1039/c8gc02918k
    日期:——
    A highly selective Ph3P-mediated C(α)–P coupling reaction of quinone monoacetals with secondary phosphine oxides is developed to provide an effective method for the synthesis of a wide array of ortho-phosphinylphenols in good to excellent yields. This protocol can be adopted for scale-up synthesis directly from cheap and abundant phenols, and the products can be easily obtained in high yields by simple
    已开发出一种高选择性的Ph 3 P介导的醌单缩醛与仲氧化膦的C(α)-P偶联反应,为合成多种正膦基苯酚提供了一种有效的方法,收率好至极好。该方案可直接用于由廉价和丰富的苯酚进行大规模合成,并且无需使用有机萃取或色谱法即可通过简单的过滤轻松轻松地以高收率获得产物。
  • Three‐Component Reaction of <i>p</i> ‐Quinone Monoacetals, Amines and Diarylphosphine Oxides to Afford <i>m‐</i> (Phosphinyl)anilides
    作者:Ruwei Shen、Xin Wang、Shunlin Zhang、Chao Dong、Dunru Zhu、Li‐Biao Han
    DOI:10.1002/adsc.201901421
    日期:2020.2.21
    The three‐component reaction of p‐quinone monoacetals, amines and diarylphosphine oxides is developed to afford m‐(diarylphosphinyl)anilides in moderate to high yields. The reaction may proceed via a process involving phospha‐nucleophilic addition to an iminoquinone acetal intermediate and/or carbonyl‐amine condensation with a phosphinyl enone intermediate.
    对苯二酚缩醛,胺和二芳基膦氧化物的三组分反应得以发展,从而以中等至高收率提供了间二芳基膦基苯胺。该反应可以通过以下过程进行:将膦酰基亲核试剂加至亚基醌缩醛中间体和/或羰基胺与次膦酰基烯酮中间体的缩合反应。
  • [EN] PHOSPHINYL AMIDINE COMPOUNDS, METAL COMPLEXES, CATALYST SYSTEMS, AND THEIR USE TO OLIGOMERIZE OR POLYMERIZE OLEFINS<br/>[FR] COMPOSÉS DE PHOSPHINYLAMIDINE, COMPLEXES DE MÉTAL, SYSTÈMES DE CATALYSEUR, ET LEUR UTILISATION POUR OLIGOMÉRISER OU POLYMÉRISER DES OLÉFINES
    申请人:CHEVRON PHILLIPS CHEMICAL CO
    公开号:WO2011082192A1
    公开(公告)日:2011-07-07
    N2-phosphinyl amidine compounds, N2-phosphinyl amidinates, N2-phosphinyl amidine metal salt complexes, N2-phosphinyl amidinate metal salt complexes are described. Methods for making N2-phosphinyl amidine compounds, N2-phosphinyl amidinates, N2-phosphinyl amidine metal salt complexes, and N2-phosphinyl amidinate metal salt complexes are also disclosed. Catalyst systems utilizing the N2-phosphinyl amidine metal salt complexes and N2-phosphinyl amidinate metal salt complexes are also disclosed along with the use of the N2-phosphinyl amidine compounds, N2-phosphinyl amidinates, N2-phosphinyl amidine metal salt complexes, and N2-phosphinyl amidinate metal salt complexes for the oligomerization and/or polymerization of olefins.
    描述了N2-膦胺化合物、N2-膦胺酸盐、N2-膦胺属盐络合物、N2-膦胺酸盐属盐络合物。还公开了制备N2-膦胺化合物、N2-膦胺酸盐、N2-膦胺属盐络合物和N2-膦胺酸盐属盐络合物的方法。还公开了利用N2-膦胺属盐络合物和N2-膦胺酸盐属盐络合物的催化剂系统,以及利用N2-膦胺化合物、N2-膦胺酸盐、N2-膦胺属盐络合物和N2-膦胺酸盐属盐络合物进行烯烃的寡聚和/或聚合的用途。
  • [EN] PHOSPHINYL FORMAMIDINE COMPOUNDS, METAL COMPLEXES, CATALYST SYSTEMS, AND THEIR USE TO OLIGOMERIZE OR POLYMERIZE OLEFINS<br/>[FR] COMPOSÉS PHOSPHINYL FORMAMIDINE, COMPLEXES MÉTALLIQUES, SYSTÈMES DE CATALYSEUR, ET LEUR UTILISATION POUR OLIGOMÉRISER OU POLYMÉRISER DES OLÉFINES
    申请人:CHEVRON PHILLIPS CHEMICAL CO
    公开号:WO2015094207A1
    公开(公告)日:2015-06-25
    N2-phosphinyl formamidine compounds and N2-phosphinyl formamidine metal salt complexes are described. Methods for making N2-phosphinyl formamidine compounds and N2-phosphinyl formamidine metal salt complexes are also disclosed. Catalyst systems utilizing the N2-phosphinyl formamidine metal salt complexes are also disclosed along with the use of the N2-phosphinyl amidine compounds and N2- phosphinyl amidinate metal salt complexes for the oligomerization and/or polymerization of olefins.
    描述了N2-酰基甲酰胺化合物和N2-酰基甲酰胺属盐配合物。还公开了制备N2-酰基甲酰胺化合物和N2-酰基甲酰胺属盐配合物的方法。还公开了利用N2-酰基甲酰胺属盐配合物的催化剂体系,以及利用N2-酰基胺化合物和N2-酰基胺属盐配合物进行烯烃的寡聚和/或聚合的用途。
查看更多

同类化合物

(βS)-β-氨基-4-(4-羟基苯氧基)-3,5-二碘苯甲丙醇 (S,S)-邻甲苯基-DIPAMP (S)-(-)-7'-〔4(S)-(苄基)恶唑-2-基]-7-二(3,5-二-叔丁基苯基)膦基-2,2',3,3'-四氢-1,1-螺二氢茚 (S)-盐酸沙丁胺醇 (S)-3-(叔丁基)-4-(2,6-二甲氧基苯基)-2,3-二氢苯并[d][1,3]氧磷杂环戊二烯 (S)-2,2'-双[双(3,5-三氟甲基苯基)膦基]-4,4',6,6'-四甲氧基联苯 (S)-1-[3,5-双(三氟甲基)苯基]-3-[1-(二甲基氨基)-3-甲基丁烷-2-基]硫脲 (R)富马酸托特罗定 (R)-(-)-盐酸尼古地平 (R)-(-)-4,12-双(二苯基膦基)[2.2]对环芳烷(1,5环辛二烯)铑(I)四氟硼酸盐 (R)-(+)-7-双(3,5-二叔丁基苯基)膦基7''-[((6-甲基吡啶-2-基甲基)氨基]-2,2'',3,3''-四氢-1,1''-螺双茚满 (R)-(+)-7-双(3,5-二叔丁基苯基)膦基7''-[(4-叔丁基吡啶-2-基甲基)氨基]-2,2'',3,3''-四氢-1,1''-螺双茚满 (R)-(+)-7-双(3,5-二叔丁基苯基)膦基7''-[(3-甲基吡啶-2-基甲基)氨基]-2,2'',3,3''-四氢-1,1''-螺双茚满 (R)-(+)-4,7-双(3,5-二-叔丁基苯基)膦基-7“-[(吡啶-2-基甲基)氨基]-2,2”,3,3'-四氢1,1'-螺二茚满 (R)-3-(叔丁基)-4-(2,6-二苯氧基苯基)-2,3-二氢苯并[d][1,3]氧杂磷杂环戊烯 (R)-2-[((二苯基膦基)甲基]吡咯烷 (R)-1-[3,5-双(三氟甲基)苯基]-3-[1-(二甲基氨基)-3-甲基丁烷-2-基]硫脲 (N-(4-甲氧基苯基)-N-甲基-3-(1-哌啶基)丙-2-烯酰胺) (5-溴-2-羟基苯基)-4-氯苯甲酮 (5-溴-2-氯苯基)(4-羟基苯基)甲酮 (5-氧代-3-苯基-2,5-二氢-1,2,3,4-oxatriazol-3-鎓) (4S,5R)-4-甲基-5-苯基-1,2,3-氧代噻唑烷-2,2-二氧化物-3-羧酸叔丁酯 (4S,4''S)-2,2''-亚环戊基双[4,5-二氢-4-(苯甲基)恶唑] (4-溴苯基)-[2-氟-4-[6-[甲基(丙-2-烯基)氨基]己氧基]苯基]甲酮 (4-丁氧基苯甲基)三苯基溴化磷 (3aR,8aR)-(-)-4,4,8,8-四(3,5-二甲基苯基)四氢-2,2-二甲基-6-苯基-1,3-二氧戊环[4,5-e]二恶唑磷 (3aR,6aS)-5-氧代六氢环戊基[c]吡咯-2(1H)-羧酸酯 (2Z)-3-[[(4-氯苯基)氨基]-2-氰基丙烯酸乙酯 (2S,3S,5S)-5-(叔丁氧基甲酰氨基)-2-(N-5-噻唑基-甲氧羰基)氨基-1,6-二苯基-3-羟基己烷 (2S,2''S,3S,3''S)-3,3''-二叔丁基-4,4''-双(2,6-二甲氧基苯基)-2,2'',3,3''-四氢-2,2''-联苯并[d][1,3]氧杂磷杂戊环 (2S)-(-)-2-{[[[[3,5-双(氟代甲基)苯基]氨基]硫代甲基]氨基}-N-(二苯基甲基)-N,3,3-三甲基丁酰胺 (2S)-2-[[[[[((1S,2S)-2-氨基环己基]氨基]硫代甲基]氨基]-N-(二苯甲基)-N,3,3-三甲基丁酰胺 (2S)-2-[[[[[[((1R,2R)-2-氨基环己基]氨基]硫代甲基]氨基]-N-(二苯甲基)-N,3,3-三甲基丁酰胺 (2-硝基苯基)磷酸三酰胺 (2,6-二氯苯基)乙酰氯 (2,3-二甲氧基-5-甲基苯基)硼酸 (1S,2S,3S,5S)-5-叠氮基-3-(苯基甲氧基)-2-[(苯基甲氧基)甲基]环戊醇 (1S,2S,3R,5R)-2-(苄氧基)甲基-6-氧杂双环[3.1.0]己-3-醇 (1-(4-氟苯基)环丙基)甲胺盐酸盐 (1-(3-溴苯基)环丁基)甲胺盐酸盐 (1-(2-氯苯基)环丁基)甲胺盐酸盐 (1-(2-氟苯基)环丙基)甲胺盐酸盐 (1-(2,6-二氟苯基)环丙基)甲胺盐酸盐 (-)-去甲基西布曲明 龙蒿油 龙胆酸钠 龙胆酸叔丁酯 龙胆酸 龙胆紫-d6 龙胆紫