18298-00-5 ((Phosphine,hexyldiphenyl-)

快速询单

结构式：

Phosphine,hexyldiphenyl-MOL文件

CAS号：

18298-00-5

英文名称：

Phosphine,hexyldiphenyl-

分子式：

C₁₈H₂₃P

分子量：

270.348985910416

Phosphine,hexyldiphenyl-(18298-00-5)名称与标识符

名称

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;AC4950;MFCD00015284;Phosphine, hexyldiphenyl-;diphenylphosphino hexan;SCHEMBL620466;DTXCID4093857;

标识符

MDL：

MFCD00015284

InChIKey：

WHNGQRQJGDUZPJ-UHFFFAOYSA-N

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：

P(C1C=CC=CC=1)(C1C=CC=CC=1)CCCCCC

Phosphine,hexyldiphenyl-(18298-00-5)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 : 0Å²

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上海瀚思化工有限公司	18939883912 021-34536277	顾经理	3003949364	询单
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金锦乐（湖南）化学有限公司		金锦乐	1226360695	询单
上海源叶生物科技有限公司	15026964105 15026964105	汤思磊	2881489226	询单

Phosphine,hexyldiphenyl-(18298-00-5)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