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Product Name:tributyl(furan-2-yl)stannane

IUPAC Name:tributyl(furan-2-yl)stannane

CAS:118486-94-5
Molecular Formula:C16H30OSn
Purity:97%
Catalog Number:CM105191
Molecular Weight:357.13

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CM105191-25g in stock ??
CM105191-100g in stock ?ň?

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Product Details

CAS NO:118486-94-5
Molecular Formula:C16H30OSn
Melting Point:-
Smiles Code:CCCC[Sn](CCCC)(CCCC)C1=CC=CO1
Density:
Catalog Number:CM105191
Molecular Weight:357.13
Boiling Point:
MDL No:MFCD00192512
Storage:

Category Infos

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.
Furan | C4H4O | Where to Buy Furans-Chemenu
Furane | Furanes | Furfuran | Furan | C4H4O | Furan Synthesis | Where to Buy Furans
Looking to buy furan? Chemenu offers a diverse selection of high-quality furan compounds. Find the perfect furans for your research or industrial applications. Explore our inventory today!

Column Infos

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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