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1,3-bis((bis((hydroxymethyl)phosphino)propyl)thio)propane | 188107-64-4

中文名称
——
中文别名
——
英文名称
1,3-bis((bis((hydroxymethyl)phosphino)propyl)thio)propane
英文别名
[2-[3-[2-[Bis(hydroxymethyl)phosphanyl]ethylsulfanyl]propylsulfanyl]ethyl-(hydroxymethyl)phosphanyl]methanol
1,3-bis((bis((hydroxymethyl)phosphino)propyl)thio)propane化学式
CAS
188107-64-4
化学式
C11H26O4P2S2
mdl
——
分子量
348.405
InChiKey
CLOULLDPUUYAES-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
  • 重原子数:
    19
  • 可旋转键数:
    14
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    132
  • 氢给体数:
    4
  • 氢受体数:
    6

反应信息

  • 作为反应物:
    描述:
    二(氰基苯)二氯化钯1,3-bis((bis((hydroxymethyl)phosphino)propyl)thio)propane二氯甲烷 为溶剂, 以90%的产率得到[2-[3-[2-[bis(hydroxymethyl)phosphanyl]ethylsulfanyl]propylsulfanyl]ethyl-(hydroxymethyl)phosphanyl]methanol;dichloropalladium
    参考文献:
    名称:
    第一水溶性二硫代双(膦)配体[(HOH(2)C)(2)P(CH(2))(2)SXS(CH(2))(2)P( CH(2)OH)(2)](X =(CH(2))(3)或C(6)H(4))。[Pd(HOH(2)C)(2)P(CH(2))(2)S(CH(2))(3)S(CH(2))(2)P( CH(2)OH)(2)](Cl)(2)(1)。
    摘要:
    硫醚官能化的水溶性双(膦)(HOH(2)C)(2)PCH(2)CH(2)S(CH(2))(3)SCH(2)CH(2)P (CH(2)OH)(2)(9)和C(6)H(4){1,2-SCH(2)CH(2)P(CH(2)OH)(2)}(2) (10)是在乙醇中存在甲醛的情况下,通过将适当的膦氢化物甲酰化而以接近定量的产率合成的。9和10与Pt(COD)Cl(2)和Pd(C(6)H(5)CN)(2)Cl(2)在双相介质(水/有机)中的反应产生水溶性Pt( II)和Pd(II)配合物[Pt(HOH(2)C)(2)P(CH(2))(2)S(CH(2))(3)S(CH(2))(2) P(CH(2)OH)(2)](Cl)(2)(11),[Pd(HOH(2)C)(2)P(CH(2))(2)S(CH(2) )(3)S(CH(2))(2)P(CH(2)OH)(2)](Cl)(2)(12),[Pt {(C(6)H(4)){
    DOI:
    10.1021/ic961319g
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文献信息

  • Radiolabeled GRPR-antagonists for diagnostic imaging and treatment of GRPR-positive cancer
    申请人:Advanced Accelerator Applications International SA
    公开号:US11083805B2
    公开(公告)日:2021-08-10
    The present invention relates to probes for use in the detection, imaging, diagnosis, targeting, treatment, etc. of cancers expressing the gastrin releasing peptide receptor (GRPR). For example, such probes may be molecules conjugated to detectable labels which are preferably moieties suitable for detection by gamma imaging and SPECT or by positron emission tomography (PET) or magnetic resonance imaging (MRI) or fluorescence spectroscopy or optical imaging methods.
    本发明涉及用于表达胃泌素释放肽受体(GRPR)的癌症的检测、成像、诊断、靶向、治疗等的探针。例如,这种探针可以是与可检测标签连接的分子,这些标签最好是适合通过伽马成像和 SPECT 或正电子发射断层扫描(PET)或磁共振成像(MRI)或荧光光谱或光学成像方法进行检测的分子。
  • Syntheses and Characterization of Chemically Flexible, Water-Soluble Dithio−Bis(phosphine) Compounds:  (HOH<sub>2</sub>C)<sub>2</sub>P(CH<sub>2</sub>)<sub>2</sub>S(CH<sub>2</sub>)<sub>3</sub>S(CH<sub>2</sub>)<sub>2</sub>P(CH<sub>2</sub>OH)<sub>2</sub>, (HOH<sub>2</sub>C)<sub>2</sub>PCH<sub>2</sub>CH<sub>2</sub>S(CH<sub>2</sub>)<sub>4</sub>SCH<sub>2</sub>CH<sub>2</sub>P(CH<sub>2</sub>OH)<sub>2</sub>, and (HOH<sub>2</sub>C)<sub>2</sub>PCH<sub>2</sub>CH<sub>2</sub>CH<sub>2</sub>S(CH<sub>2</sub>)<sub>3</sub>SCH<sub>2</sub>CH<sub>2</sub>CH<sub>2</sub>P(CH<sub>2</sub>OH)<sub>2</sub>. Systematic Investigation of the Effect of Chain Length on the Coordination Chemistry of Rhenium(V). X-ray Crystal Structures of [ReO<sub>2</sub>(HOH<sub>2</sub>C)<sub>2</sub>P(CH<sub>2</sub>)<sub>2</sub>S(CH<sub>2</sub>)<sub>3</sub>S(CH<sub>2</sub>)<sub>2</sub>P(CH<sub>2</sub>OH)<sub>2</sub>]<sub>2</sub>(Cl)<sub>2</sub>, [ReO<sub>2</sub>(HOH<sub>2</sub>C)<sub>2</sub>P(CH<sub>2</sub>)<sub>2</sub>S(CH<sub>2</sub>)<sub>4</sub>S(CH<sub>2</sub>)<sub>2</sub>P-(CH<sub>2</sub>OH)<sub>2</sub>]<sub>2</sub>(ReO<sub>4</sub><sup>-</sup>)<sub>2</sub>, and [ReO<sub>2</sub>(HOH<sub>2</sub>C)<sub>2</sub>P(CH<sub>2</sub>)<sub>3</sub>S(CH<sub>2</sub>)<sub>3</sub>S(CH<sub>2</sub>)<sub>3</sub>P(CH<sub>2</sub>OH)<sub>2</sub>](Cl)
    作者:C. Jeffrey Smith、Kattesh V. Katti、Wynn A. Volkert、Leonard J. Barbour
    DOI:10.1021/ic970097z
    日期:1997.8.1
    The water-soluble dithio-bis(phosphine)s (HOH2C)(2)P(CH2)(2)S(CH2)(2)P(CH2OH)(2) (1), (HOH2C)(2)PCH2- CH2S(CH2)(4)SCH2CH2P(CH2OH)(2) (4), and (HOH2C)(2)PCH2CH2CH2S(CH2)(3)SCH2CH2CH2P(CH2OH)(2) (7) were synthesized in near-quantitative yield by the formylation of their appropriate phosphine hydride precursors in the presence of formaldehyde and oxygen-free ethanol. The reactions of 1, 4, and 7 with [ReO2(C5H5N)(4)](Cl) in refluxing water produced the water-soluble Re(V) complexes [ReO2(HOH2C)(2)P(CH2)(2)S(CH2)(3)S(CH2)(2)P(CH2OH)(2)](2)(Cl)(2) (8), [ReO2(HOH2C)(2)P(CH2)(2)S(CH2)(4)S(CH2)(2)P(CH2OH)(2)](2)(ReO4-)(2) (9), and [ReO2(HOH2C)(2)P-(Cl-2)(3)S (CH2)(3)S(CH2)(3)P(CH2OH)(2)](Cl) (10) The X-ray crystallographic analysis of 8-10, reported in this paper, confirmed the dioxorhenium(V) structures. All of the compounds were characterized by H-1, C-13, and P-31 NMR spectroscopy. HPLC chromatographic analysis of 8-10 demonstrated purities of >98% for each of the new complexes formed. X-ray data for [ReO2(HOH2C)(2)P(CH2)(2)S(CH2)(3)S(CH2)(2)P(CH2OH)(2)](2)(Cl)(2) (8): monoclinic, P2(1)/n, a = 10.7982(5) Angstrom, b = 23.486(1) Angstrom, c = 15.4408(8) Angstrom, beta = 94.539(1)degrees, Z = 4, R = 0.0246 (wR2 = 0.0574). For [ReO2(HOH2C)(2)P(CH2)(2)S(CH2)(4)S(CH2)(2)P(CH2OH)(2)](2)(ReO4-)(2) (9): triclinic, <(P)over bar 1>, a = 10.3762(5) Angstrom, b = 12.1099(6) Angstrom, c = 18.7555(9) Angstrom, alpha = 90.259(1)degrees, beta = 91.900(1)degrees, gamma = 104,965(1)degrees, Z = 2, R = 0.0546 (wR2 = 0.1412). For [ReO2(HOH2C)(2)P(CH2)(3)S(CH2)(3)S(CH2)(3)P(CH2OH)(2)] (10): monoclinic, P2(1)/n, a = 10.6224(6) Angstrom, b = 12.5532(8) Angstrom, c = 18.5757(11) Angstrom, beta = 103.663(10)degrees, Z = 4, R = 0.0261 (wR2 = 0.0656).
  • Synthesis and Coordination Chemistry of the First Water-Soluble Dithio−Bis(phosphine) Ligands [(HOH<sub>2</sub>C)<sub>2</sub>P(CH<sub>2</sub>)<sub>2</sub>S−X−S(CH<sub>2</sub>)<sub>2</sub>P(CH<sub>2</sub>OH)<sub>2</sub>] (X = (CH<sub>2</sub>)<sub>3</sub> or C<sub>6</sub>H<sub>4</sub>). X-ray Crystal Structure of [Pd(HOH<sub>2</sub>C)<sub>2</sub>P(CH<sub>2</sub>)<sub>2</sub>S(CH<sub>2</sub>)<sub>3</sub>S(CH<sub>2</sub>)<sub>2</sub>P(CH<sub>2</sub>OH)<sub>2</sub>](Cl)<sub>2</sub><sup>1</sup>
    作者:C. Jeffrey Smith、V. Sreenivasa Reddy、Srinivasa R. Karra、Kattesh V. Katti、Leonard J. Barbour
    DOI:10.1021/ic961319g
    日期:1997.4.1
    (aqueous/organic) produced the water-soluble Pt(II) and Pd(II) complexes [Pt(HOH(2)C)(2)P(CH(2))(2)S(CH(2))(3)S(CH(2))(2)P(CH(2)OH)(2)](Cl)(2) (11), [Pd(HOH(2)C)(2)P(CH(2))(2)S(CH(2))(3)S(CH(2))(2)P(CH(2)OH)(2)](Cl)(2) (12), [Pt(C(6)H(4))1,2-S(CH(2))(2)P(CH(2)OH)(2)}(2)}](Cl)(2) (13), and [Pd(C(6)H(4))1,2-S(CH(2))(2)P(CH(2)OH)(2)}(2)}](Cl)(2) (14) in near quantitative yields. The X-ray crystal structure
    硫醚官能化的水溶性双(膦)(HOH(2)C)(2)PCH(2)CH(2)S(CH(2))(3)SCH(2)CH(2)P (CH(2)OH)(2)(9)和C(6)H(4)1,2-SCH(2)CH(2)P(CH(2)OH)(2)}(2) (10)是在乙醇中存在甲醛的情况下,通过将适当的膦氢化物甲酰化而以接近定量的产率合成的。9和10与Pt(COD)Cl(2)和Pd(C(6)H(5)CN)(2)Cl(2)在双相介质(水/有机)中的反应产生水溶性Pt( II)和Pd(II)配合物[Pt(HOH(2)C)(2)P(CH(2))(2)S(CH(2))(3)S(CH(2))(2) P(CH(2)OH)(2)](Cl)(2)(11),[Pd(HOH(2)C)(2)P(CH(2))(2)S(CH(2) )(3)S(CH(2))(2)P(CH(2)OH)(2)](Cl)(2)(12),[Pt (C(6)H(4))
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