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4390-39-0

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4390-39-0 Usage

General Description

9-Azabicyclo[3.3.1]nonan-3-one, also known as 9-azabicyclononan-3-one or 9-azabicyclo[3.3.1]nonan-3-one, is a bicyclic compound containing an azabicyclo[3.3.1]nonane skeleton with a ketone functional group at position 3. It is a key intermediate in the synthesis of various pharmaceuticals, including antipsychotic and anticonvulsant drugs. 9-Azabicyclo[3.3.1]nonan-3-one is also used as a building block in organic synthesis, particularly in the preparation of heterocyclic compounds. Its unique structure and reactivity make it a valuable tool in medicinal and synthetic chemistry. Additionally, its derivatives have shown potential as anti-inflammatory and anticancer agents.

Check Digit Verification of cas no

The CAS Registry Mumber 4390-39-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,3,9 and 0 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 4390-39:
(6*4)+(5*3)+(4*9)+(3*0)+(2*3)+(1*9)=90
90 % 10 = 0
So 4390-39-0 is a valid CAS Registry Number.
InChI:InChI=1/C8H13NO/c10-8-4-6-2-1-3-7(5-8)9-6/h6-7,9H,1-5H2

4390-39-0Upstream product

4390-39-0Relevant articles and documents

Metabolism of N-alkyldiamines and N-alkylnortropinones by transformed root cultures of Nicotiana and Brugmansia

Boswell, Henry D.,Draeger, Birgit,Eagles, John,McClintock, Carol,Parr, Adrian,Portsteffen, Andreas,Robins, David J.,Robins, Richard J.,Walton, Nicholas J.,Wong, Chi

, p. 855 - 869 (2007/10/03)

A range of analogues of N-methylputrescine and tropinone were fed to transformed root cultures of Nicotiana rustica and/or a Brugmansia candida x aurea hybrid. These cultures were made by the transformation of the relevant plant species with Agrobacterium rhizogenes. A number of the metabolites, notably those showing a relatively modest alteration in the N-alkyl substituent, were metabolized in vivo to form homologues of the normal alkaloids biosynthesized by these roots. These products were identified by GC/MS and comparison with some synthetic reference materials. Analogues with major alterations in the size of the N-alkyl substituent were not metabolized at all. In the N. rustica cultures, the analogues fed at 1 mM significantly affected the profile of normal alkaloids, with up to a 4-fold diminution in nicotine being found in the presence of N-n-propylputrescine. The ratio between alkaloids of the pyrrolidine series and the piperideine series was also affected. In contrast, the presence of the analogues in the B. candida x aurea hybrid culture at 1 mM did not inhibit or substantially interfere with the accumulation of the normal spectrum of alkaloids. The potential for using these cultures to make complex novel products from simple precursors is discussed.

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