Название продукции:8-(tert-Butoxycarbonyl)-1-oxa-2,8-diazaspiro-[4.5]dec-2-ene-3-carboxylic acid

IUPAC Name:8-[(tert-butoxy)carbonyl]-1-oxa-2,8-diazaspiro[4.5]dec-2-ene-3-carboxylic acid

CAS:479636-66-3
Молекулярная формула:C13H20N2O5
Чистота:95%
Номер в каталоге:CM138912
Молекулярная масса:284.31

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Информация о продукции

Номер CAS:479636-66-3
Молекулярная формула:C13H20N2O5
Точка плавления:-
Smiles-код:O=C(C1=NOC2(CCN(C(OC(C)(C)C)=O)CC2)C1)O
Плотность:
Номер в каталоге:CM138912
Молекулярная масса:284.31
Точка кипения:
Номер Mdl:MFCD12198539
Хранение:Store at 2-8°C.

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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Isoxazolines
Isoxazolines are a class of five-membered heterocyclic chemical compounds, containing one atom each of oxygen and nitrogen which are located adjacent to one another. Compounds containing an isoxazoline ring have a variety of uses with many being biologically active.

Column Infos

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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