基本信息 |
|
| 产品名称： | 二[三(4-(十七氟辛基)苯基)膦]二氯化钯(II) |
| CAS： | 326475-44-9 |
| 中文同义词： | 二[三(4-(十七氟辛基)苯基)膦]二氯化钯(II) |
| 英文同义词： | BIS[TRIS(4-(HEPTADECAFLUOROOCTYL)PHENYL)PHOSPHINE]PALLADIUM(II) DICHLORIDE ; BIS[TRIS(4-(PERFLUOROOCTYL)PHENYL)PHOSPHINE]PALLADIUM(II) DICHLORIDE |
| MDL号： | MFCD04040059 |
| 氢键受体数量： | 0 |
| 氢键供体数量： | 0 |
| Smile： | c1cc(ccc1C(C(C(CC(C(C(C(F)(F)F)(F)F)(F)F)(F)F)(F)F)(F)F)(F)F)P(c2ccc(cc2)C(C(C(C(C(C(C(C(F)(F)F)(F)F)(F)F)(F)F)(F)F)(F)F)(F)F)(F)F)c3ccc(cc3)C(C(C(C(C(C(C(C(F)(F)F)(F)F)(F)F)(F)F)(F)F)(F)F)(F)F)(F)F.c1cc(ccc1C(C(C(C(C(C(C(C(F)(F)F)(F)F)(F)F)(F)F)(F)F)(F)F)(F)F)(F)F)P(c2ccc(cc2)C(C(C(C(C(C(C(C(F)(F)F)(F)F)(F)F)(F)F)(F)F)(F)F)(F)F)(F)F)c3ccc(cc3)C(C(C(C(C(C(C(C(F)(F)F)(F)F)(F)F)(F)F)(F)F)(F)F)(F)F)(F)F.Cl[Pd]Cl |
| InChi： | InChI=1S/C42H12F51P.C42H14F49P.2ClH.Pd/c43-19(44,22(49,50)25(55,56)28(61,62)31(67,68)34(73,74)37(79,80)40(85,86)87)13-1-7-16(8-2-13)94(17-9-3-14(4-10-17)20(45,46)23(51,52)26(57,58)29(63,64)32(69,70)35(75,76)38(81,82)41(88,89)90)18-11-5-15(6-12-18)21(47,48)24(53,54)27(59,60)30(65,66)33(71,72)36(77,78)39(83,84)42(91,92)93;43-20(44,13-21(45,46)26(55,56)37(77,78)40(83,84)85)25(53,54)22(47,48)14-1-7-17(8-2-14)92(18-9-3-15(4-10-18)23(49,50)27(57,58)29(61,62)31(65,66)33(69,70)35(73,74)38(79,80)41(86,87)88)19-11-5-16(6-12-19)24(51,52)28(59,60)30(63,64)32(67,68)34(71,72)36(75,76)39(81,82)42(89,90)91;;;/h1-12H;1-12H,13H2;2*1H;/q;;;;+2/p-2 |
| InChiKey： | InChIKey=IYLQGUPYTFHEPL-UHFFFAOYSA-L |
性质 |
|
| 注解： | APPLICATION: CATALYST FOR STILLE AND SUZUKI COUPLINGS IN ''FLUOROUS BIPHASE SYSTEMS'' (FBS) ASSAY METHOD: 31P-NMR OTHER NOTES: PERFLUORO-TAGGED PD COMPLEXES AS CATALYSTS FOR STILLE COUPLINGS IN A FLUOROUS BIPHASE SYSTEM,1 PALLADIUM-CATALYZED SUZUKI COUPLINGS UNSPSC: 12352100 WGK: 3 |
安全信息 |
|
* If the product has intellectual property rights, a license granted is must or contact us.
2010-2025 © Chemical Cloud Database. ALL Rights Reserved.浙ICP备11020424号-1
浙公网安备 33010802004002号
English![二[三(4-(十七氟辛基)苯基)膦]二氯化钯(II)](http://www.chemcd.com/createImage?smile=c1cc%28ccc1C%28C%28C%28CC%28C%28C%28C%28F%29%28F%29F%29%28F%29F%29%28F%29F%29%28F%29F%29%28F%29F%29%28F%29F%29%28F%29F%29P%28c2ccc%28cc2%29C%28C%28C%28C%28C%28C%28C%28C%28F%29%28F%29F%29%28F%29F%29%28F%29F%29%28F%29F%29%28F%29F%29%28F%29F%29%28F%29F%29%28F%29F%29c3ccc%28cc3%29C%28C%28C%28C%28C%28C%28C%28C%28F%29%28F%29F%29%28F%29F%29%28F%29F%29%28F%29F%29%28F%29F%29%28F%29F%29%28F%29F%29%28F%29F.c1cc%28ccc1C%28C%28C%28C%28C%28C%28C%28C%28F%29%28F%29F%29%28F%29F%29%28F%29F%29%28F%29F%29%28F%29F%29%28F%29F%29%28F%29F%29%28F%29F%29P%28c2ccc%28cc2%29C%28C%28C%28C%28C%28C%28C%28C%28F%29%28F%29F%29%28F%29F%29%28F%29F%29%28F%29F%29%28F%29F%29%28F%29F%29%28F%29F%29%28F%29F%29c3ccc%28cc3%29C%28C%28C%28C%28C%28C%28C%28C%28F%29%28F%29F%29%28F%29F%29%28F%29F%29%28F%29F%29%28F%29F%29%28F%29F%29%28F%29F%29%28F%29F.Cl%5BPd%5DCl&size=web.jpg)
