Produktname:methyl 3-boc-3-azabicyclo[3.1.1]heptane-6-carboxylate

IUPAC Name:3-tert-butyl 6-methyl 3-azabicyclo[3.1.1]heptane-3,6-dicarboxylate

CAS:1363380-75-9
Molekulare Formel:C13H21NO4
Reinheit:95%+
Katalognummer:CM106617
Molekulargewicht:255.31

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Produkt-Details

CAS-Nr.:1363380-75-9
Molekulare Formel:C13H21NO4
Schmelzpunkt:-
SMILES-Code:O=C(C1C2CN(C(OC(C)(C)C)=O)CC1C2)OC
Dichte:
Katalognummer:CM106617
Molekulargewicht:255.31
Siedepunkt:
Mdl-Nr.:
Lagerung:Keep in a dry and a tight container and store at 2°C~8°C,protect from light

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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Bridged Compounds
Bridged ring compound refers to any two rings in the compound, which share two non-directly connected carbon atoms, and are classified into bicyclic hydrocarbons, tricyclic hydrocarbons, tetracyclic hydrocarbons, etc. Carbon atoms used in two or more rings are bridgehead carbon atoms, and the bond connecting the bridgehead carbon atoms is called a bridge. Bridged ring compounds are a class of organic compounds that are widely present in nature and usually have important physiological activities, such as the famous anticancer drug paclitaxel and antimalarial drug artemisinin.
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Cyclobutanes
The molecular structure of cyclobutane has four carbon atoms, and its four carbon atoms are not in the same plane, which is the folded conformation of cyclobutane. Cyclobutane itself is not of commercial or biological interest, but more complex derivatives are important in biology and biotechnology. Currently, nine FDA-approved drugs contain the cyclobutane structure. From the perspective of therapeutic areas, cyclobutyl drugs are mainly distributed in popular areas such as tumors, neurological diseases, infectious diseases, endocrine and metabolic diseases.

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