174470-67-8 Usage
Chemical Class
Pyrazolidines This compound belongs to the class of pyrazolidines, which are heterocyclic organic compounds consisting of a five-membered ring with one nitrogen atom and four carbon atoms.
Structure
Ethyl Ester Derivative It is an ethyl ester derivative of 5,5-dimethyl-3-oxo-1-pyrazolidinecarboxylic acid, which means it has an ethoxy group (-OCH2CH3) attached to the pyrazolidine ring.
Molecular Weight
193.25 g/mol The molecular weight is the mass of one mole of the compound, calculated by adding the atomic weights of all the atoms in the molecular formula.
Pharmacological Properties
Potential pharmacological properties This compound is used in organic synthesis and drug development due to its potential pharmacological properties.
Building Block in Synthesis
Pharmaceutical compounds It is commonly used as a building block in the synthesis of various pharmaceutical compounds for the treatment of various diseases.
Research and Applications
Material science, agriculture, and other fields Research is ongoing to explore the potential applications of this compound in fields such as material science, agriculture, and other areas beyond pharmaceuticals.
Check Digit Verification of cas no
The CAS Registry Mumber 174470-67-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,4,4,7 and 0 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 174470-67:
(8*1)+(7*7)+(6*4)+(5*4)+(4*7)+(3*0)+(2*6)+(1*7)=148
148 % 10 = 8
So 174470-67-8 is a valid CAS Registry Number.
174470-67-8Relevant articles and documents
Synthesis, insecticidal and anti-acetylcholinesterase activity of a new class of heterocyclic methanesulfonates
Holan, George,Virgona, Chris T.,Watson, Keith G.,Finkelstein, Bruce L.
, p. 77 - 80 (2007/10/03)
A series of 3-methanesulfonyloxy-2-pyrazolines were prepared by mesylation of the corresponding pyrazolidin-3-ones. The compounds exhibited strong insecticidal and anti-acetylcholinesterase activity.
