646055-79-0 Usage
Explanation
The compound consists of 9 carbon atoms, 15 hydrogen atoms, 1 nitrogen atom, and 2 oxygen atoms.
Explanation
The compound is derived from 1-azabicyclo[2.2.1]heptane-2-carboxylic acid by replacing the hydroxyl group (-OH) with an ethoxy group (-OCH3).
Explanation
Due to its unique structure and properties, this compound is commonly used as an intermediate in the synthesis of various drugs and pharmaceuticals.
Explanation
The compound serves as a reference standard in analytical chemistry and research, helping to calibrate instruments and validate experimental methods.
Explanation
The chemical properties and structure of 1-azabicyclo[2.2.1]heptane-2-carboxylic acid, ethyl ester (9CI) make it suitable for a wide range of applications, particularly in the fields of drug development and research.
Structure
Ester form of 1-azabicyclo[2.2.1]heptane-2-carboxylic acid
Application in pharmaceutical industry
Building block for drug synthesis
Use as a reference standard
Analytical chemistry and research
Suitability for various applications
Drug development and research
Check Digit Verification of cas no
The CAS Registry Mumber 646055-79-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,4,6,0,5 and 5 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 646055-79:
(8*6)+(7*4)+(6*6)+(5*0)+(4*5)+(3*5)+(2*7)+(1*9)=170
170 % 10 = 0
So 646055-79-0 is a valid CAS Registry Number.
646055-79-0Relevant articles and documents
THE USE OF N-ARYL DIAZASPIRACYCLIC COMPOUNDS IN THE TREATMENT OF ADDICTION
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Page/Page column 66, (2010/10/20)
Compounds, compositions and methods for treating drug addiction, nicotine addiction, and/or obesity are disclosed. The compounds are N-aryl diazaspirocyclic compounds, bridged analogs of N-heteraryl diazaspirocyclic compounds, or prodrugs or metabolites of these compounds. The aryl group can be a five- or six-membered heterocyclic ring (heteroaryl). The compounds are effective at inhibiting dopamine production and/or secretion, and accordingly are effective at inhibiting the physiological "reward" process that is associated with ingestion of nicotine and/or illicit drugs. The compounds and compositions can be administered in effective amounts to inhibit dopamine release, wihout resulting in appreciable adverse side effects (e.g., side effects such as significant increases in blood pressure and heart rate, significant negative effects upon the gastro-intestinal tract, and significant effects upon skeletal muscle).