Nom du produit:Tri(furan-2-yl)phosphine
IUPAC Name:tris(furan-2-yl)phosphane
- CAS：5518-52-5
- Formule moléculaire：C12H9O3P
- Pureté：98%
- Numéro de catalogue：CM196106
- Poids moléculaire：232.17
Pour une utilisation en R&D uniquement..
Détails du produit
- N° CAS:5518-52-5
- Formule moléculaire:C12H9O3P
- Point de fusion:-
- Code SMILES:P(C1=CC=CO1)(C2=CC=CO2)C3=CC=CO3
- Densité:
- Numéro de catalogue:CM196106
- Poids moléculaire:232.17
- Point d'ébullition:286.4°C at 760 mmHg
- N° Mdl:MFCD00151857
- Stockage:Keep in Inert atmosphere, store at 2-8°C.
Category Infos
- Catalysts and Ligands
- A catalyst refers to a substance that increases the rate of a reaction without changing the overall standard Gibbs free energy change of the reaction. Ligands represent atoms, molecules, and ions that can bond with a central atom (metal or metalloid). In general, ligands will donate at least one electron when participating in a bond. Two-phase catalysis of catalysts and ligands is the first application in the field of fluorine chemistry. The method of self-fluorine two-phase catalysis has developed rapidly, and a large number of new fluorine-based catalysts and ligands (especially phosphines) have been obtained in the field of chemistry.
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- Furans
- Furan is a cyclic flammable liquid compound C4H4O that is obtained from wood oils of pines or made synthetically and is used especially in organic synthesis. Furan is aromatic because a pair of lone pair electrons of the oxygen atom in its molecule forms a large π bond in the plane of the conjugated orbital, making a total of 6 electrons in the plane of the conjugated plane, conforming to the 4n+2 structure. Aromaticity makes furan have the property of easy substitution and difficult addition. The other lone pair of electrons in oxygen stretches out. The oxygen atom itself conforms to sp2 hybridization. Due to the presence of the aromatic ring, the chemical behavior of furan is not very similar to that of other unsaturated heterocycles. The oxygen in the aromatic ring has an electron-donating effect, so the electrophilic substitution reactivity of furan is stronger than that of benzene.
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- Furane | Furanes | Furfuran | Furan | C4H4O | Furan Synthesis | Where to Buy Furans
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