Nom du produit:tert-butyl 9-amino-3-azaspiro[5.5]undecane-3-carboxylate

IUPAC Name:tert-butyl 9-amino-3-azaspiro[5.5]undecane-3-carboxylate

CAS:1272758-41-4
Formule moléculaire:C15H28N2O2
Pureté:97%
Numéro de catalogue:CM106364
Poids moléculaire:268.4

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Détails du produit

N° CAS:1272758-41-4
Formule moléculaire:C15H28N2O2
Point de fusion:-
Code SMILES:O=C(N1CCC2(CCC(N)CC2)CC1)OC(C)(C)C
Densité:
Numéro de catalogue:CM106364
Poids moléculaire:268.4
Point d'ébullition:
N° Mdl:
Stockage:

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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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Cyclohexanes
Cyclohexane is an organic compound with a chemical formula C6H12. It is a colorless liquid with a pungent odor, insoluble in water, and soluble in most organic solvents such as ethanol, ether, benzene, and acetone. Cyclohexyl fragments are a common structure in both natural and synthetic drugs. It can be used as both core structure and part of achiral side chain.

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