17613-25-1 Usage
Description
3-(3,4-dihydroisoquinolin-2(1H)-yl)-3-oxopropanenitrile is a chemical compound characterized by the molecular formula C13H12N2O2. It is a nitrile compound that features both an isoquinoline and a ketone functional group, making it a versatile building block in organic synthesis.
Uses
Used in Pharmaceutical and Medicinal Industry:
3-(3,4-dihydroisoquinolin-2(1H)-yl)-3-oxopropanenitrile is used as a building block for the preparation of various pharmaceutical and medicinal products due to its unique structural features and potential biological activity.
Used in Organic Synthesis:
3-(3,4-dihydroisoquinolin-2(1H)-yl)-3-oxopropanenitrile is used as a precursor for the synthesis of other nitrogen-containing compounds, contributing to the development of new chemical entities with potential applications in various fields.
Used in Drug Discovery and Development:
3-(3,4-dihydroisoquinolin-2(1H)-yl)-3-oxopropanenitrile is utilized as a potential candidate for drug discovery and development, owing to its pharmacological properties and the possibility of it exhibiting biological activity that could be harnessed for therapeutic purposes.
Check Digit Verification of cas no
The CAS Registry Mumber 17613-25-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,6,1 and 3 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 17613-25:
(7*1)+(6*7)+(5*6)+(4*1)+(3*3)+(2*2)+(1*5)=101
101 % 10 = 1
So 17613-25-1 is a valid CAS Registry Number.
17613-25-1Relevant articles and documents
Synthesis of perhydro-N-(2,2-disubstituted- 3-aminopropyl) heterocycles as potentially bioactive compounds and fragments for combinatorial chemistry
Hayotsyan, Sargis S.,Mkryan, Gevorg G.,Aghekyan, Asya A.,Melikyan, Gagik S.
, p. 189 - 192 (2013/01/16)
A new method for the preparation of perhydro- N - (2,2-disubstituted-3- aminopropyl) heterocycles that allows to obtain a large variety of corresponding derivatives with high to moderate yields using simple procedures is described.
