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(2-Brom-phenyl)-phenyl-phosphin | 92576-86-8

中文名称
——
中文别名
——
英文名称
(2-Brom-phenyl)-phenyl-phosphin
英文别名
<2-Brom-phenyl>-phenyl-phosphin;(2-Bromophenyl)-phenylphosphane
(2-Brom-phenyl)-phenyl-phosphin化学式
CAS
92576-86-8
化学式
C12H10BrP
mdl
——
分子量
265.089
InChiKey
WBNGYVVEMNWMQQ-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):
    3.7
  • 重原子数:
    14
  • 可旋转键数:
    2
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    0
  • 氢给体数:
    0
  • 氢受体数:
    0

文献信息

  • [EN] BIDENTATE CHIRAL LIGANDS FOR USE IN CATALYTIC ASYMMETRIC ADDITION REACTIONS<br/>[FR] LIGANDS CHIRAUX BIDENTATES UTILISABLES DANS DES RÉACTIONS D'ADDITION CATALYTIQUES ASYMÉTRIQUES
    申请人:SOLVIAS AG
    公开号:WO2009065784A1
    公开(公告)日:2009-05-28
    Compounds of the formula (I), in the form of mixtures comprising predominantly one diastereomer or in the form of pure diastereomers, Z1-Q-P*R0R1 (I) in which Z1 is a C-bonded, secondary phosphine group -P(R)2; in which R is in each case independently hydrocarbon radicals or heterohydrocarbon radicals, or Z1 is the -P*R0R1 group; Q is a bivalent, achiral, aromatic base skeleton, a bivalent, achiral ferrocene base skeleton, an optionally substituted bivalent cycloalkane or heterocycloalkane skeleton, or a C1-C4-alkylene skeleton, and in which base skeletons a secondary phosphine group Z1 is bonded directly to a carbon atom, or, in the case of cyclic base skeletons, directly to a carbon atom or via a C1-C4-alkylene group, and in which base skeletons a P-chiral group -P*R0R1 is bonded directly to a carbon atom, or, in the case of cyclic base skeletons, directly to a carbon atom or via a C1-C4-alkylene group to a carbon atom such that the phosphorus atoms are linked via 1 to 7 atoms of a carbon chain optionally interrupted by heteroatoms from the group of O, S, N, Fe or Si; P* is a chiral phosphorus atom; R0 is methyl or hydroxyl, and R0 is methyl when Z1 is the -P*R0R1 group; and R1 is a C-bonded optically enriched or optically pure chiral, mono- or polycyclic, nonaromatic hydrocarbon or heterohydrocarbon radical which has 3 to 12 ring atoms and 1 to 4 rings and which has a stereogenic carbon atom at least in the α position to the P-C bond; Metal complexes of these ligands are homogeneous catalysts for asymmetric addition reactions, particularly hydrogenations.
    化合物的公式(I)的形式,以主要包含一种对映异构体的混合物形式或纯对映异构体的形式,Z1-Q-P*R0R1(I),其中Z1是C-键合的次磷酸基团-P(R)2;其中R分别是烃基或杂烃基,或Z1是-P*R0R1基团;Q是二价的、不对映的、芳香基骨架,二价的、不对映的二茂铁基骨架,一个可选择取代的二价环烷烃或杂环烷烃骨架,或一个C1-C4-烷基骨架,并且在这些基骨架中,次磷酸基团Z1直接键合到一个碳原子,或者在环状基骨架的情况下,直接键合到一个碳原子或通过一个C1-C4-烷基团,以及在这些基骨架中,一个P-手性基团-P*R0R1直接键合到一个碳原子,或者在环状基骨架的情况下,直接键合到一个碳原子或通过一个C1-C4-烷基团到一个碳原子,以使原子通过1到7个碳链原子连接,这些碳链原子可以通过来自O、S、N、Fe或Si的杂原子间断连接;P*是一个手性原子;R0是甲基或羟基,当Z1是-P*R0R1基团时,R0是甲基;R1是一个C-键合的光学富集或光学纯的手性、单环或多环、非芳香烃基或杂烃基,具有3到12个环原子和1到4个环,并且至少在P-C键的α位置具有一个立体异构碳原子;这些配体属络合物是用于不对称加成反应的均相催化剂,特别是氢化反应。
  • BIDENTATE CHIRAL LIGANDS FOR USE IN CATALYTIC ASYMMETRIC ADDITION REACTIONS
    申请人:Pugin Benoît
    公开号:US20110118482A1
    公开(公告)日:2011-05-19
    Compounds of the formula (I), in the form of mixtures comprising predominantly one diastereomer or in the form of pure diastereomers, Z 1 -Q-P*R 0 R 1 (I) in which Z 1 is a C-bonded, secondary phosphine group —P(R) 2 ; in which R is in each case independently hydrocarbon radicals or heterohydrocarbon radicals, or Z 1 is the —P*R 0 R 1 group; Q is a bivalent, achiral, aromatic base skeleton, a bivalent, achiral ferrocene base skeleton, an optionally substituted bivalent cycloalkane or heterocycloalkane skeleton, or a C 1 -C 4 -alkylene skeleton, and in which base skeletons a secondary phosphine group Z 1 is bonded directly to a carbon atom, or, in the case of cyclic base skeletons, directly to a carbon atom or via a C 1 -C 4 -alkylene group, and in which base skeletons a P-chiral group —P*R 0 R 1 is bonded directly to a carbon atom, or, in the case of cyclic base skeletons, directly to a carbon atom or via a C 1 -C 4 -alkylene group to a carbon atom such that the phosphorus atoms are linked via 1 to 7 atoms of a carbon chain optionally interrupted by heteroatoms from the group of O, S, N, Fe or Si; P* is a chiral phosphorus atom; R 0 is methyl or hydroxyl, and R 0 is methyl when Z 1 is the —P*R 0 R 1 group; and R 1 is a C-bonded optically enriched or optically pure chiral, mono- or polycyclic, nonaromatic hydrocarbon or heterohydrocarbon radical which has 3 to 12 ring atoms and 1 to 4 rings and which has a stereogenic carbon atom at least in the a position to the P—C bond; Metal complexes of these ligands are homogeneous catalysts for asymmetric addition reactions, particularly hydrogenations.
    化合物的结构式(I),以主要由一个对映异构体组成的混合物形式或纯对映异构体形式出现,其中Z1是一个C-键结合的次级膦基团- P(R)2;其中R在每种情况下独立地是碳氢基团或杂环碳氢基团,或Z1是-P * R0R1基团;Q是双价的、无手性的、芳香基骨架、双价的、无手性的二茂铁基骨架、可选地取代的双价环烷基或杂环烷基骨架,或C1-C4-烷基骨架,在这些基骨架中,次级膦基团Z1直接键合到一个碳原子上,或在环状基骨架的情况下,直接键合到一个碳原子或通过C1-C4-烷基骨架键合到一个碳原子上,且在这些基骨架中,P-手性基团-P * R0R1直接键合到一个碳原子上,或在环状基骨架的情况下,直接键合到一个碳原子或通过C1-C4-烷基骨架键合到一个碳原子,使得原子通过1到7个碳链原子(可选地由O、S、N、Fe或Si的杂原子中断)相连;P *是一个手性原子;R0是甲基或羟基,当Z1是-P * R0R1基团时,R0为甲基;R1是C-键结合的光学纯或光学富集的手性、单环或多环、非芳香碳氢或杂环碳氢基团,具有3到12个环原子和1到4个环,并且在P-C键的α位至少有一个立体异构碳原子;这些配体属络合物是不对称加成反应的均相催化剂,特别是氢化反应。
  • P-CHIROGENIC ORGANOPHOSPHORUS COMPOUNDS
    申请人:CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE (CNRS)
    公开号:US20140142325A1
    公开(公告)日:2014-05-22
    Novel P-chirogenic organophosphorus compounds of general formula (I), a process for the synthesis of the compounds of formula (I), and intermediate products of general formulae (II), (III) and (IV), as shown below, are involved in the synthesis of compounds (I). Metal complexes including compounds (I) as ligands are also described. The novel compounds and complexes are useful in asymmetric catalysis by transition metal complexes or organocatalysis, especially for asymmetric hydrogenation or allylation. Compounds of general formula (I) may be useful as agrochemical and therapeutic substances, or as reagents or intermediates for fine chemistry.
    通式为(I)的新型P-手性有机化合物的合成方法,以及通式为(II)、(III)和(IV)的中间体,如下所示,参与了化合物(I)的合成。还描述了以化合物(I)为配体属配合物。这些新型化合物和配合物在过渡属配合物或有机催化剂的不对称催化中非常有用,特别是在不对称氢化或烯丙基化中。通式为(I)的化合物可能在农药和治疗物质中有用,或作为精细化学的试剂或中间体。
  • US8450501B2
    申请人:——
    公开号:US8450501B2
    公开(公告)日:2013-05-28
  • US8598371B2
    申请人:——
    公开号:US8598371B2
    公开(公告)日:2013-12-03
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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