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Phosphine,hexyldiphenyl- | 18298-00-5

Phosphine,hexyldiphenyl-结构式图片|18298-00-5结构式图片
Phosphine,hexyldiphenyl-
18298-00-5
C18H23P
270.34902
如需查看该化合物的详细结构式,mol文件,smile,InChi 请点击:Phosphine,hexyldiphenyl-结构式
87564
名称和标识符
MDL MFCD00015284
InChIKey WHNGQRQJGDUZPJ-UHFFFAOYSA-N
Inchi InChI=1S/C18H23P/c1-2-3-4-11-16-19(17-12-7-5-8-13-17)18-14-9-6-10-15-18/h5-10,12-15H,2-4,11,16H2,1H3
SMILES C(P(C1C=CC=CC=1)C1C=CC=CC=1)CCCCC
别名信息
- 中文别名 -
  • 己基二苯基膦
- 英文别名 -
  • Phosphine,hexyldiphenyl-
  • hexyl(diphenyl)phosphane
  • hexyldiphenylphosphine
  • Einecs 242-180-5
  • NS00051500
  • WHNGQRQJGDUZPJ-UHFFFAOYSA-N
  • A921516
  • DTXSID60171366
  • n-hexyldiphenylphosphine
  • HEXYLDIPHENYLPHOSPHANE
  • SY235507
  • 18298-00-5
  • EINECS 242-180-5
  • AC4950
  • MFCD00015284
  • Phosphine, hexyldiphenyl-
  • diphenylphosphino hexan
  • SCHEMBL620466
  • Hexyldiphenylphosphine
物化性质
实验特性
LogP 4.69960
PSA 0
沸点 362°Cat760mmHg
闪点 181.5°C
密度 g/cm3
计算特性
精确分子量 270.15389
氢键供体数量 0
氢键受体数量 0
可旋转化学键数量 7
同位素质量 270.154
重原子数量 19
复杂度 196
同位素原子数量 0
确定原子立构中心数量 0
不确定原子立构中心数量 0
确定化学键立构中心数量 0
不确定化学键立构中心数量 0
共价键单元数量 1
疏水参数计算参考值(XlogP) 5.4
拓扑分子极性表面积 0Ų
相关文献
  • 1. Crystal and molecular structure of di-μ-carbonyl-dicarbonyl[cyclohexyl(diphenyl)phosphine](π-methylcylopentadienylnickelio)cobalt
    Ian L. C. Campbell,Frederick S. Stephens J. Chem. Soc. Dalton Trans. 1975 337
  • 2. Stereochemically controlled synthesis of unsaturated alcohols by the Horner–Wittig reaction
    Peter M. Ayrey,Michael A. Bolton,Antony D. Buss,Nicholas Greeves,Daniel Levin,Paul Wallace,Stuart Warren J. Chem. Soc. Perkin Trans. 1 1992 3407
  • 3. Stereochemical control (E/Z and syn/anti) by the diphenylphosphinoyl group in the synthesis of allylic alcohols by allylic rearrangement and by 1,4-diastereoselective reduction of enones
    Jonathan Clayden,Eric W. Collington,Jason Elliott,Stephen J. Martin,Andrew B. McElroy,Stuart Warren,David Waterson J. Chem. Soc. Perkin Trans. 1 1993 1849
  • 4. Control over absolute (R,S), relative (syn,anti) and geometrical (E,Z) stereochemistry in the synthesis of allylically substituted alkenes from diphenylphosphinoyl epoxy alcohols
    Jonathan Clayden,Andrew B. McElroy,Stuart Warren J. Chem. Soc. Perkin Trans. 1 1995 1913
  • 5. The thermal decomposition of phosphonium alkoxides
    C. T. Eyles,S. Trippett J. Chem. Soc. C 1966 67
  • 6. The synthesis of (Z)-penta-2,4-dien-1-ol and substituted (E)-pentadienols by the stereochemically controlled Horner–Wittig reaction
    Paul S. Brown,Nicholas Greeves,Andrew B. McElroy,Stuart Warren J. Chem. Soc. Perkin Trans. 1 1991 1485
  • 7. Abnormal reactions of the betaines R3PCH2·CH(ō)·R
    S. Trippett,B. J. Walker J. Chem. Soc. C 1966 887
  • 8. Reactions of sodium hydride with ω-hydroxyalkyl-phosphonium, -arsonium and -ammonium salts
    A. R. Hands,A. J. H. Mercer J. Chem. Soc. C 1968 1331
  • 9. Regioselectivity and control in alkene formation from a carbonium ion after diphenylphosphinoyl migration
    Alan H. Davidson,Ian Fleming,J. Ian Grayson,Andrew Pearce,Roger L. Snowden,Stuart Warren J. Chem. Soc. Perkin Trans. 1 1977 550
  • 10. Organic synthesis using diphenylphosphinoyl as a migrating functional group: diene synthesis
    Alan H. Davidson,Stuart Warren J. Chem. Soc. Perkin Trans. 1 1976 639
专业数据库参考
PubChemId 87564
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