1232136-97-8 Usage
Explanation
The molecular formula represents the number of atoms of each element present in a molecule. In this case, the compound has 8 carbon (C) atoms, 13 hydrogen (H) atoms, and 3 nitrogen (N) atoms.
Explanation
The compound features a cyclopropyl ring, which is a three-membered carbon ring, and a pyrazole group, a five-membered ring containing four carbon atoms and one nitrogen atom.
Explanation
1-(5-cyclopropyl-1H-pyrazol-3-yl)-N-methylmethanamine is a derivative of methylmethanamine, meaning it is structurally related and has been modified from the parent compound.
Explanation
The compound is used in the research and development of new drugs, particularly those targeting the central nervous system.
Explanation
Due to its unique structure and properties, the compound is considered a valuable candidate for the development of new therapeutic agents.
Explanation
More research is needed to fully comprehend the compound's pharmacological effects, which will help determine its potential applications in the medical field.
Structure
Cyclopropyl ring and pyrazole group
Derivative
Methylmethanamine
Application
Pharmaceutical research and development
Therapeutic potential
Valuable candidate for potential therapeutic applications
Further research
Necessary to understand pharmacological effects and potential uses in medicine
Check Digit Verification of cas no
The CAS Registry Mumber 1232136-97-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,3,2,1,3 and 6 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1232136-97:
(9*1)+(8*2)+(7*3)+(6*2)+(5*1)+(4*3)+(3*6)+(2*9)+(1*7)=118
118 % 10 = 8
So 1232136-97-8 is a valid CAS Registry Number.
1232136-97-8Relevant academic research and scientific papers
Synthesis of 3-aminomethyl-substituted pyrazoles and isoxazoles
Musatov,Starodubtseva,Rakishev,Turova,Vinogradov
experimental part, p. 1199 - 1203 (2011/12/15)
A series of new 3-(aminomethyl)pyrazoles and 3-(aminomethyl)isoxazoles was synthesized along a route involving the formation as key intermediates of esters of 5-substituted 1H-pyrazole-3-carboxylic and 1H-isoxazole-3-carboxylic acids. All compounds obtain
