cas 146514-35-4|| where to buy tert-butyl (2-oxotetrahydrofuran-3-yl)carbamate

Nombre del producto:tert-butyl (2-oxotetrahydrofuran-3-yl)carbamate

IUPAC Name:tert-butyl N-(2-oxooxolan-3-yl)carbamate

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CM127493-50mg	in stock	Ƕưũ
CM127493-100mg	in stock	ũǜũ
CM127493-250mg	in stock	Ⱥǜũ
CM127493-500mg	in stock	Ǝǜũ
CM127493-1g	in stock	ưțư
CM127493-5g	in stock	ǊƦŵ
CM127493-10g	in stock	ǶƎưǊ

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: Núm. De CAS :146514-35-4; Fórmula molecular:C9H15NO4; Punto de fusión:-; Código de sonrisas:O=C(OC(C)(C)C)NC1C(OCC1)=O; Densidad:

: Número de catálogo:CM127493; Peso molecular:201.22; Punto de ebullición:; Nº Mdl:; Almacenamiento:Store at 2-8°C.

: Tetrahydrofurans; Tetrahydrofuran is a heterocyclic organic compound with the molecular formula C4H8O. Tetrahydrofuran belongs to ethers and is the complete hydrogenation product of furan. It is a colorless, water-miscible organic liquid with small viscosity at normal temperature and pressure. Because of its long liquid range, it is a commonly used medium polar aprotic solvent. Its main use is as a precursor of high molecular polymers.

: 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.