Nombre del producto:8-(4-bromo-2-chlorobenzyl)-1,4-dioxa-8-azaspiro[4.5]decane

IUPAC Name:8-[(4-bromo-2-chlorophenyl)methyl]-1,4-dioxa-8-azaspiro[4.5]decane

CAS:1704074-50-9
Fórmula molecular:C14H17BrClNO2
Pureza:95%
Número de catálogo:CM105319
Peso molecular:346.65

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Detalles del producto

Núm. De CAS :1704074-50-9
Fórmula molecular:C14H17BrClNO2
Punto de fusión:-
Código de sonrisas:ClC1=CC(Br)=CC=C1CN1CCC2(CC1)OCCO2
Densidad:
Número de catálogo:CM105319
Peso molecular:346.65
Punto de ebullición:
Nº Mdl:
Almacenamiento:

Category Infos

Piperidines
Piperidine is an azacycloalkane that is cyclohexane in which one of the carbons is replaced by a nitrogen. Although piperidine is a common organic compound, it is an immensely important class of compounds medicinally: the piperidine ring is the most common heterocyclic subunit among FDA approved drugs.
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Spiro Compounds
A spiro compound is a polycyclic compound in which two monocyclic rings share one carbon atom; the shared carbon atom is called a spiro atom. Spiro compounds have rigid structures, stable structures, and have special properties that general organic compounds do not possess, such as anomeric effect, spiro conjugation and spiro hyperconjugation. Compared with the monocyclic structure or the planar aromatic structure, the spiro structure has a larger three-dimensional structure; the heterocyclic spiro structure is also regarded as the biological isostere of some groups, which can change the drug to a certain extent. The water solubility, lipophilicity, dominant conformation and ADMET properties of the molecule make the optimized lead molecule easier to drug. Therefore, spiro compounds occupy a very important position in drug development.
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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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