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3-Oxo-2-quinuclidinecarboxylic acid ethyl ester is a chemical compound with the molecular formula C12H17NO3. It belongs to the family of quinuclidines, which are compounds comprising a quinuclidine moiety, a bicyclic heterocycle made up of a pyridine and a piperidine joined by sharing a nitrogen atom. 3-Oxo-2-quinuclidinecarboxylic acid ethyl ester is primarily used in chemical and pharmaceutical research, with its detailed properties, including physical and chemical attributes, potential health effects, and safety handling precautions, typically found in its corresponding Material Safety Data Sheet provided by the manufacturer or supplier.

34286-16-3

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34286-16-3 Usage

Uses

Used in Chemical Research:
3-Oxo-2-quinuclidinecarboxylic acid ethyl ester is used as a research compound for the synthesis and study of various chemical structures and reactions. Its unique bicyclic heterocycle structure makes it a valuable building block in the development of new chemical entities.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 3-Oxo-2-quinuclidinecarboxylic acid ethyl ester is used as a key intermediate in the synthesis of potential drug candidates. Its presence in the quinuclidine family suggests that it may have applications in the development of medications targeting the central nervous system or other therapeutic areas.
Used in Material Safety Data Sheets:
3-Oxo-2-quinuclidinecarboxylic acid ethyl ester is referenced in Material Safety Data Sheets (MSDS) to provide essential information on its physical and chemical properties, potential health hazards, and safety precautions for handling and storage. This information is crucial for researchers and professionals working with the compound to ensure safe laboratory practices and compliance with regulatory requirements.

Check Digit Verification of cas no

The CAS Registry Mumber 34286-16-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,2,8 and 6 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 34286-16:
(7*3)+(6*4)+(5*2)+(4*8)+(3*6)+(2*1)+(1*6)=113
113 % 10 = 3
So 34286-16-3 is a valid CAS Registry Number.

34286-16-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 3-oxo-1-azabicyclo[2.2.2]octane-2-carboxylate

1.2 Other means of identification

Product number -
Other names 3-Chinuclidon-2-carbonsaeure-ethylester

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:34286-16-3 SDS

34286-16-3Relevant academic research and scientific papers

Preparation method of quininone derivative

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Paragraph 0047-0050, (2020/04/06)

The invention provides a preparation method of a quininone derivative, and belongs to the field of pharmaceutical chemical industry. According to the method disclosed by the invention, the 3-quininonederivative is obtained by taking a diethanolamine derivative as a starting material through chlorination or methanesulfonic acid and diethyl malonate cyclization and Dieckmann Condensation. The product produced by the method has the characteristics of high purity, high yield, low cost, simple operation and stable process.

Preparation method of optical activity 3-quinuclidinol

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Paragraph 0011; 0012, (2018/04/03)

The invention relates to an intermediate synthesis method, belongs to the field of organic synthesis, and particularly relates to a preparation method of optical activity 3-quinuclidinol with the advantages that the operation is simple and convenient, the cost is low, and the method is suitable for industrial production. An intermediate of 3-quinuclidinol is obtained by using 4-nipecotic acid as astarting material through esterification, nucleophilic substitution, Dieckmann condensation, decarboxylation, salification, reduction, acetylization, chemical resolution and the like. The reaction formula is shown in the description.

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