Product Name:((5-(1,3-Dioxolan-2-yl)furan-2-yl)ethynyl)trimethylsilane

IUPAC Name:{2-[5-(1,3-dioxolan-2-yl)furan-2-yl]ethynyl}trimethylsilane

CAS:342601-16-5
Molecular Formula:C12H16O3Si
Purity:97%
Catalog Number:CM213949
Molecular Weight:236.34

Packing Unit Available Stock Price($) Quantity
CM213949-1g 3-4 Weeks Əǭǭǭ
CM213949-5g 3-4 Weeks ƏŽřţ
CM213949-10g 3-4 Weeks ƏƴƏǟ

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Product Details

CAS NO:342601-16-5
Molecular Formula:C12H16O3Si
Melting Point:-
Smiles Code:C[Si](C)(C#CC1=CC=C(C2OCCO2)O1)C
Density:
Catalog Number:CM213949
Molecular Weight:236.34
Boiling Point:
MDL No:
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
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Dioxolanes
Dioxolane is a heterocyclic acetal with the formula (CH2)2O2CH2. It is related to tetrahydrofuran by exchanging an oxygen for the CH2 group. The isomer 1,2-dioxolane (in which the two oxygen centers are adjacent) is a peroxide. 1,3-Dioxolane is used as solvent and comonomer in polyacetal. The dioxolane-type and their hydrogenolysis can provide very valuable partially protected building blocks either for oligosaccharide syntheses or sugar transformations.

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