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Bis-(p-chlorphenyl)-chlormethylphosphinoxid | 13685-36-4

中文名称
——
中文别名
——
英文名称
Bis-(p-chlorphenyl)-chlormethylphosphinoxid
英文别名
1-Chloro-4-[chloromethyl-(4-chlorophenyl)phosphoryl]benzene
Bis-(p-chlorphenyl)-chlormethylphosphinoxid化学式
CAS
13685-36-4
化学式
C13H10Cl3OP
mdl
——
分子量
319.555
InChiKey
ZDOFKYHAGYDKBL-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

物化性质

  • 熔点:
    98-100 °C
  • 沸点:
    387.5±37.0 °C(Predicted)
  • 密度:
    1.41±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    4.4
  • 重原子数:
    18
  • 可旋转键数:
    3
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.08
  • 拓扑面积:
    17.1
  • 氢给体数:
    0
  • 氢受体数:
    1

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量
  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    Bis-(p-chlorphenyl)-chlormethylphosphinoxidsodium hydroxide三氯硅烷 作用下, 以 甲醇氯仿N,N-二甲基甲酰胺 为溶剂, 反应 73.5h, 生成 [Bis-(4-chloro-phenyl)-phosphanyl]-methanethiol
    参考文献:
    名称:
    Staudinger Ligation of Peptides at Non-Glycyl Residues
    摘要:
    The Staudinger ligation provides a means to form an amide bond between a phosphinothioester and azide. This reaction holds promise for the ligation of peptides en route to the total chemical synthesis of proteins. (Diphenylphosphino) methanethiol is the most efficacious of known reagents for mediating the Staudinger ligation of peptides, providing high (> 90%) isolated yields for equimolar couplings in which a glycine residue is at the nascent junction. Surprisingly, the yields are lower (< 50%) for non-glycyl couplings due to an aza-Wittig reaction that diverts the reaction toward a phosphonamide byproduct. Here, the partitioning of the reaction toward Staudinger ligation (and away from the aza-Wittig reaction) is shown to increase with increasing electron density on phosphorus. This electron density can be tuned either by installing functional groups on the phenyl substituents of (diphenylphosphino) methanethiol or by changing the polarity of the solvent. Installing p-methoxy groups and using a solvent of low polarity (such as toluene or dioxane) provide especially high (> 80%) isolated yields for the ligation of two non-glycyl residues. These conditions retain the high chemoselectivity of the reaction and do not lead to a substantial change in reaction rate. The traceless Staudinger ligation is now poised to enable the iterative ligation of peptides with little regard for their sequence, as well as the synthesis of amide bonds for other purposes.
    DOI:
    10.1021/jo0620056
  • 作为产物:
    描述:
    Bis(4-chlorophenyl)(hydroxymethyl)phosphine oxide五氯化磷 作用下, 以 为溶剂, 反应 0.5h, 以91%的产率得到Bis-(p-chlorphenyl)-chlormethylphosphinoxid
    参考文献:
    名称:
    Patsanovskii, I. I.; Ishmaeva, E. A.; Sundukova, E. N., Journal of general chemistry of the USSR, 1986, vol. 56, # 3, p. 501 - 509
    摘要:
    DOI:
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文献信息

  • On the Preparation of Carbohydrate−Protein Conjugates Using the Traceless Staudinger Ligation
    作者:Cyrille Grandjean、Alain Boutonnier、Catherine Guerreiro、Jean-Michel Fournier、Laurence A. Mulard
    DOI:10.1021/jo0505472
    日期:2005.9.1
    The nature of a linker used for preparing glycoconjugate vaccines is of utmost importance as it may lead to immunogenic biomolecules. We report the conjugation of carbohydrate haptens to protein carriers leading to potential vaccines using the traceless Staudinger ligation. The ligation relies on the selective transfer of a phosphane substituent to an azide to form a native amide bond in the final product upon release of an oxidized phosphane byproduct. We designed new phosphino-functionalized cross-linkers suitable for protein carrier derivatization. We evaluated their utility in preparing conjugates using both synthetic and purified bacterial carbohydrates. The use of a borane-protected phosphane which is deprotected at the time of the ligation reaction led to the best results observed thus far in terms of stability toward oxidation and reactivity.
  • Tsvetkov, E. N.; Tkachenko, S. E.; Yarkevich, A. N., Bulletin de la Societe Chimique de France, 1988, # 2, p. 339 - 341
    作者:Tsvetkov, E. N.、Tkachenko, S. E.、Yarkevich, A. N.
    DOI:——
    日期:——
  • Tkachenko, S. E.; Yarkevich, A. N.; Tsvetkov, E. N., Doklady Chemistry, 1990, vol. 315, # 1.3, p. 334 - 337
    作者:Tkachenko, S. E.、Yarkevich, A. N.、Tsvetkov, E. N.、Galkin, V. I.、Sayakhov, R. D.、et al.
    DOI:——
    日期:——
  • PATSANOVSKIJ, I. I.;ISHMAEVA, EH. A.;SUNDUKOVA, E. N.;YARKEVICH, A. N.;TS+, ZH. OBSHCH. XIMII, 1986, 56, N 3, 567-576
    作者:PATSANOVSKIJ, I. I.、ISHMAEVA, EH. A.、SUNDUKOVA, E. N.、YARKEVICH, A. N.、TS+
    DOI:——
    日期:——
  • US3989824A
    申请人:——
    公开号:US3989824A
    公开(公告)日:1976-11-02
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