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![[(二(1-金刚烷基)丁基膦基)-2-(2′-氨基-1,1′-联苯基)]钯(II)甲磺酸酯 95%](/deepweb/assets/sigmaaldrich/product/structures/391/492/af15708b-9501-44ae-a25f-d3574589a865/640/af15708b-9501-44ae-a25f-d3574589a865.png)
化驗
95%
形狀
solid
反應適用性
reaction type: Buchwald-Hartwig Cross Coupling Reaction
reaction type: Heck Reaction
reaction type: Hiyama Coupling
reaction type: Negishi Coupling
reaction type: Sonogashira Coupling
reaction type: Stille Coupling
reaction type: Suzuki-Miyaura Coupling
reagent type: ligand
mp
60-61 °C (lit.)
官能基
phosphine
SMILES 字串
C1CCC(CC1)P(C2CCCCC2)c3ccccc3
InChI
1S/C18H27P/c1-4-10-16(11-5-1)19(17-12-6-2-7-13-17)18-14-8-3-9-15-18/h1,4-5,10-11,17-18H,2-3,6-9,12-15H2
InChI 密鑰
VPLLTGLLUHLIHA-UHFFFAOYSA-N
Tatyana I Rokitskaya et al.
Biochimica et biophysica acta. Biomembranes, 1863(1), 183483-183483 (2020-10-02)
To clarify the contribution of charge delocalization in a lipophilic ion to the efficacy of its permeation through a lipid membrane, we compared the behavior of alkyl derivatives of triphenylphosphonium, tricyclohexylphosphonium and trihexylphosphonium both in natural and artificial membranes. Exploring
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