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9-Azabicyclo[3.3.1]nonan-3-one, 9-ethylis a chemical compound with a bicyclic structure containing a nitrogen atom. It is commonly used as a building block and intermediate in the synthesis of pharmaceutical compounds and agrochemicals. This chemical has been studied for its potential as a precursor in the preparation of various bioactive compounds and heterocyclic derivatives. It is also known for its potential for use as a chiral resolving agent and as a reagent for the synthesis of nitrogen-containing heterocycles. Additionally, it has been investigated for its potential in the development of novel drug candidates and as a starting material in the production of fine chemicals.

27092-59-7

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27092-59-7 Usage

Uses

Used in Pharmaceutical Industry:
9-Azabicyclo[3.3.1]nonan-3-one, 9-ethylis used as a building block and intermediate for the synthesis of pharmaceutical compounds. Its unique bicyclic structure containing a nitrogen atom allows for the development of novel drug candidates with potential therapeutic applications.
Used in Agrochemical Industry:
9-Azabicyclo[3.3.1]nonan-3-one, 9-ethylis used as a building block and intermediate for the synthesis of agrochemicals. Its potential as a precursor in the preparation of various bioactive compounds and heterocyclic derivatives makes it a valuable component in the development of new agrochemical products.
Used in Chiral Resolution:
9-Azabicyclo[3.3.1]nonan-3-one, 9-ethylis used as a chiral resolving agent. Its unique structure allows for the separation of enantiomers, which is crucial in the production of enantiomerically pure compounds for various applications, including pharmaceuticals and agrochemicals.
Used in Synthesis of Nitrogen-Containing Heterocycles:
9-Azabicyclo[3.3.1]nonan-3-one, 9-ethylis used as a reagent for the synthesis of nitrogen-containing heterocycles. Its potential for use in the preparation of various heterocyclic derivatives makes it a valuable component in the development of new chemical compounds with potential applications in various industries.
Used in Production of Fine Chemicals:
9-Azabicyclo[3.3.1]nonan-3-one, 9-ethylis used as a starting material in the production of fine chemicals. Its versatility and potential for use in the synthesis of various compounds make it an important component in the manufacture of high-quality specialty chemicals.

Check Digit Verification of cas no

The CAS Registry Mumber 27092-59-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,7,0,9 and 2 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 27092-59:
(7*2)+(6*7)+(5*0)+(4*9)+(3*2)+(2*5)+(1*9)=117
117 % 10 = 7
So 27092-59-7 is a valid CAS Registry Number.

27092-59-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 9-ethyl-9-azabicyclo[3.3.1]nonan-3-one

1.2 Other means of identification

Product number -
Other names N-Ethyl-9-aza-bicyclo<3.3.1>nonan-3-on

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:27092-59-7 SDS

27092-59-7Upstream product

27092-59-7Downstream Products

27092-59-7Relevant academic research and scientific papers

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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