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Merck

14664

Sigma-Aldrich

三苯基膦,聚合物键合

100-200 mesh, extent of labeling: ~3.2 mmol/g loading

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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About This Item

线性分子式:
-C6H4P(C6H5)2
CAS号:
分子量:
262.29
MDL號碼:
分類程式碼代碼:
12352128
PubChem物質ID:
NACRES:
NA.22

形狀

solid

品質等級

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
reaction type: solution phase peptide synthesis
reagent type: ligand

標籤範圍

~3.2 mmol/g loading

基質

crosslinked with 2% DVB

粒徑

100-200 mesh

官能基

phosphine

SMILES 字串

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 密鑰

RIOQSEWOXXDEQQ-UHFFFAOYSA-N

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應用

Polymer-bound triphenylphosphine (PPh3) is a reusable organocatalyst for the Mukaiyama aldol and Mannich reaction. It can also be used as a traceless reagent for Mitsunobu reaction in combinatorial chemistry to synthesize aryl ethers from phenols and alcohols.

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 3

個人防護裝備

dust mask type N95 (US), Eyeshields, Faceshields, Gloves


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Polymer-supported PPh 3 as a reusable organocatalyst for the Mukaiyama aldol and Mannich reaction.
Matsukawa S, et al.
Royal Society of Chemistry Advances, 4(53), 27780-27786 (2014)
Polymer-bound triphenylphosphine as traceless reagent for Mitsunobu reactions in combinatorial chemistry: Synthesis of aryl ethers from phenols and alcohols.
Tunoori A R, et al.
Tetrahedron Letters, 39(48), 8751-8754 (1998)
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Gold nanoparticles (GNPs) have considerable applications in biomedicine, such as in bio-sensing, bio-imaging, drug delivery and photothermal therapeutics. However, currently there are limited information regarding the impact of pregnancy on their biodistribution, elimination and toxicity. In this study, we investigated

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