93094
三苯基膦，聚合物键合
100-200 mesh, extent of labeling: ~1-1.5 mmol/g Capacity (Phosphor)
别名:
二苯基膦-聚苯乙烯, 聚苯乙烯交联二乙烯基苯，二苯基磷化, 苯乙烯-二乙烯基苯共聚物，二苯基磷化
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关于此项目
线性分子式:
-C6H4P(C6H5)2
化学文摘社编号:
分子量:
262.29
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352128
MDL number:
form
solid
Quality Level
reaction suitability
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, reaction type: solution phase peptide synthesis, reagent type: ligand
extent of labeling
~1-1.5 mmol/g Capacity (Phosphor)
matrix
crosslinked with 1% DVB
particle size
100-200 mesh
functional group
phosphine
storage temp.
2-8°C
SMILES string
c1ccc(cc1)P(c2ccccc2)c3ccccc3
InChI
1S/C18H15P/c1-4-10-16(11-5-1)19(17-12-6-2-7-13-17)18-14-8-3-9-15-18/h1-15H
InChI key
RIOQSEWOXXDEQQ-UHFFFAOYSA-N
General description
Triphenylphosphine, polymer-bound is polystyrene crosslinked with divinylbenzene, widely used in many organic syntheses such as peptide synthesis, heterocycle synthesis, esterification, and total synthesis. It can be easily removed from the reaction products by simple filtration.
Application
Triphenylphosphine, polymer-bound is used as a polymer support to synthesize dipeptides, olefins, aryl-alkyl ethers, and in the esterification of alkylphosphonic acids. It acts as a Lewis acid, and dehydrating agent when complexed with halogen, hence useful in the acetonation of sugars.
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存储类别
11 - Combustible Solids
wgk
WGK 3
ppe
dust mask type N95 (US), Eyeshields, Faceshields, Gloves
Synthesis of aryl ethers from aminoalcohols using polymer-supported triphenylphosphine
Tetrahedron Letters, 43, 2157-2159 (2002)
Uday Narayan Maiti et al.
ACS applied materials & interfaces, 7(46), 25898-25905 (2015-11-03)
A scalable and controllable nanoscale perforation method for graphene is developed on the basis of the two-step thermal activation of a graphene aerogel. Different resistance to the thermal oxidation between graphitic and defective domains in the weakly reduced graphene oxide
Crispin Lichtenberg et al.
Dalton transactions (Cambridge, England : 2003), 44(46), 20056-20066 (2015-11-04)
A diolefin ether, trop2O (2), and a diolefin thioether, trop2S (3), have been investigated as ligand analogues of the well-established diolefin amine, trop2NH (1). Compounds 2 and 3 form different conformers in solution and in the solid state. Whereas 2
全球贸易项目编号
| 货号 | GTIN |
|---|---|
| 180246-5G | 04061838754820 |
| 180246-25G | 04061838754813 |
| 93094-25G | 04061833418192 |
| 93094-5G | 04061833349298 |