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3,3'-(苯基膦二基)二(苯-1-磺酸)二钠

中文名称
3,3'-(苯基膦二基)二(苯-1-磺酸)二钠
中文别名
——
英文名称
Disodium;3-[phenyl-(3-sulfonatophenyl)phosphanyl]benzenesulfonate
英文别名
disodium;3-[phenyl-(3-sulfonatophenyl)phosphanyl]benzenesulfonate
3,3'-(苯基膦二基)二(苯-1-磺酸)二钠化学式
CAS
——
化学式
C18H13Na2O6PS2
mdl
——
分子量
466.4
InChiKey
PWRPHTBBQPNXQA-UHFFFAOYSA-L
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):
    -4.74
  • 重原子数:
    29
  • 可旋转键数:
    3
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    131
  • 氢给体数:
    0
  • 氢受体数:
    6

反应信息

点击查看最新优质反应信息

文献信息

  • Simultaneous imaging of cardiac perfusion and a vitronectin receptor targeted imaging agent
    申请人:——
    公开号:US20020106325A1
    公开(公告)日:2002-08-08
    The present invention describes a method of concurrent imaging in a mammal comprising: a) administering to said mammal a vitronectin receptor targeted imaging agent and a perfusion imaging agent; and b) concurrently detecting the vitronectin target imaging agent bound at the vitronectin receptor and the perfusion imaging agent; and c) forming an image from the detection of said vitronectin receptor targeted imaging agent and said perfusion imaging agent.
    本发明描述了一种在哺乳动物中进行并行成像的方法,包括: a) 向所述哺乳动物施用一个靶向维龙蛋白受体的成像剂和一个灌注成像剂;以及 b) 同时检测维龙蛋白靶向成像剂与维龙蛋白受体结合以及灌注成像剂;以及 c) 从检测到的维龙蛋白受体靶向成像剂和灌注成像剂形成图像。
  • BIS(6-METHYL-3-SULPHOPHENYL)PHENYLPHOSPHINE, AMMONIUM SALT THEREOF, AND METHOD FOR PRODUCING SAME
    申请人:HOKKO CHEMICAL INDUSTRY CO., LTD.
    公开号:US20160052947A1
    公开(公告)日:2016-02-25
    Provided are a water-soluble triarylphosphine for a palladium catalyst, which has high selectivity in a telomerization reaction and can be recovered with efficiency, an ammonium salt thereof, and a method for efficiently producing the same. Specifically, provided are bis(6-methyl-3-sulphophenyl)phenylphosphine; a bis(6-methyl-3-sulphonatophenyl)phenylphosphine diammonium salt obtained by reacting the phosphine with a tertiary amine having a total of 3 to 27 carbon atoms in groups bonded to one nitrogen atom; and a method for producing the same.
    提供了一种水溶性三芳基膦钯催化剂,其在缩聚反应中具有高选择性,并且可以高效回收,以及其铵盐,以及一种高效生产该化合物的方法。具体提供了双(6-甲基-3-磺酸苯基)苯基膦;通过将膦与含有3至27个碳原子的基团与一个氮原子键合的三级胺反应而得到的双(6-甲基-3-磺酸苯基)苯基膦二铵盐;以及一种生产该化合物的方法。
  • METHOD FOR PRODUCING 2,7-OCTADIEN-1-OL
    申请人:KURARAY CO., LTD.
    公开号:US20160046549A1
    公开(公告)日:2016-02-18
    Provided is a simple and industrially advantageous method for producing 2,7-octadien-1-ol, in which an expensive palladium catalyst is recovered in high efficiency and the reaction rate per atom of palladium is enhanced. Specifically, provided is a method for producing 2,7-octadien-1-ol by subjecting butadiene and water to a telomerization in the presence of a palladium catalyst containing a water-soluble triarylphosphine having two or more sulfonate groups in the molecule and a palladium compound, a tertiary amine, and carbon dioxide, including a step of mixing the telomerization solution obtained by the telomerization with an organic solvent having a dielectric constant at 25° C. of 2 to 18, followed by carrying out phase separation in the presence of carbon dioxide, thereby obtaining 2,7-octadien-1-ol from an organic phase while recovering an aqueous phase including the palladium catalyst. By this production method, the selectivity for 2,7-octadien-1-ol is enhanced.
    提供了一种简单且在工业上具有优势的生产2,7-辛二烯-1-醇的方法,其中昂贵的钯催化剂以高效率回收,并且增强了每个钯原子的反应速率。具体而言,提供了一种通过在存在包含具有两个或更多磺酸基团的水溶性三芳基膦和钯化合物、三级胺和二氧化碳的钯催化剂的情况下,使丁二烯和水经过缩聚反应来生产2,7-辛二烯-1-醇的方法,包括将通过缩聚反应获得的缩聚溶液与在25°C时具有介电常数为2到18的有机溶剂混合的步骤,然后在二氧化碳的存在下进行相分离,从而从有机相中获得2,7-辛二烯-1-醇,同时回收包括钯催化剂的水相。通过这种生产方法,对2,7-辛二烯-1-醇的选择性得到增强。
  • beta-DIHYDROFURAN DERIVING COMPOUND, METHOD FOR PRODUCING beta-DIHYDROFURAN DERIVING COMPOUND OR beta-TETRAHYDROFURAN DERIVING COMPOUND, beta-GLYCOSIDE COMPOUND, METHOD FOR PRODUCING beta GLYCOSIDE COMPOUND, AND METHOD FOR PRODUCING 4'-ETHYNYL D4T AND ANALOGUE COMPOUNDS THEREOF
    申请人:Iriyama Yusuke
    公开号:US20120322995A1
    公开(公告)日:2012-12-20
    The invention provides a process for producing a β-dihydrofuran derivative represented by formula (1) or a β-tetrahydrofuran derivative represented by formula (4), characterized in that the process includes causing a dialkyl dicarbonate, a diaralkyl dicarbonate, or a halide to act on a diol compound represented by formula (2) or (3). The invention also provides a process for producing 4′-ethynyl-2′,3′-didehydro-3′-deoxythymidine or an analog thereof, the process including glycosylation and deprotection.
    该发明提供了一种生产由式(1)表示的β-二氢呋喃衍生物或由式(4)表示的β-四氢呋喃衍生物的过程,其特征在于该过程包括使二烷基二碳酸酯、二芳基二碳酸酯或卤化物作用于由式(2)或(3)表示的二醇化合物。该发明还提供了一种生产4'-乙炔基-2',3'-二去氢-3'-脱氧胸苷或其类似物的过程,包括糖基化和去保护。
  • Process for producing indole compound
    申请人:Sakurai Yasuhiro
    公开号:US20070083053A1
    公开(公告)日:2007-04-12
    There is provided a novel process for producing an indole derivative which comprises cyclizing 2-nitrobenzylcarbony compound in the presence of a catalyst comprising a Group VIII metal of the Periodic Table, characterized by conducting the cyclization in a gas atmosphere containing carbon monoxide. The process enables an indole compound to be selectively produced in a high yield from 2-nitrobenzylcarbonyl compound, and hardly yields an indoline compound as a reduction by-product that has been a problem in the catalytic hydrogenation method employing a noble metal catalyst. The indole derivative produced by the present process is useful for various fine chemical intermediates including compounds and physiologically active substances such as pharmaceuticals and agrochemicals.
    提供了一种生产吲哚衍生物的新方法,包括在存在周期表第VIII族金属的催化剂的情况下,使2-硝基苄酰化合物环化,其特征在于在含有一氧化碳的气氛中进行环化。该方法使得可以从2-硝基苄酰化合物中选择性地高产率地生产吲哚化合物,并且几乎不产生吲哚啉化合物作为催化氢化方法中使用贵金属催化剂时的还原副产物,这一直是一个问题。由本方法生产的吲哚衍生物可用于各种精细化学中间体,包括药物和农药等化合物和生理活性物质。
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