124476-79-5 Usage
Molecular Structure
Contains a pyrrole ring and a carbonitrile group
Functional Groups
Amino group (NH2)
Methoxyphenyl group (C6H5O)
Carbonyl group (C=O)
Chemical Properties
Reactivity influenced by the presence of amino, methoxyphenyl, and carbonyl groups
May undergo various chemical reactions based on the functional groups present
Potential Applications
Organic synthesis: Can serve as a building block for creating complex organic molecules
Pharmaceutical research: Structure may be valuable for designing new drug compounds or studying biological processes
Further Exploration
Precise uses and properties require experimentation and analysis in a laboratory setting.
Check Digit Verification of cas no
The CAS Registry Mumber 124476-79-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,4,4,7 and 6 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 124476-79:
(8*1)+(7*2)+(6*4)+(5*4)+(4*7)+(3*6)+(2*7)+(1*9)=135
135 % 10 = 5
So 124476-79-5 is a valid CAS Registry Number.
InChI:InChI=1/C12H11N3O2/c1-17-10-4-2-9(3-5-10)15-11(16)6-8(7-13)12(15)14/h2-5H,6,14H2,1H3
124476-79-5Relevant academic research and scientific papers
Heterocyclization using phase transfer catalysis: A simple and convenient synthesis of 2-amino-1-aryl-5-oxo-4,5-dihydro-1H-pyrrole-3-carbonitriles
Dave,Parikh
, p. 1301 - 1306 (2007/10/03)
A simple and convenient synthesis of 2-amino-1-aryl-5-oxo-4,5-dihydro-1H-pyrrole-3-carbonitriles has been studied with and without phase transfer conditions. The best results were obtained using 18-crown-6 under solid-liquid phase transfer conditions in a
Synthesis and Reactions of 2-Amino-1-aryl-5-oxo-Δ2-pyrroline-3-carbonitriles
Schaefer, Harry,Gewald, Karl
, p. 315 - 322 (2007/10/02)
The reaction of malononitrile with α-chloro acetanilides 1 in presence of potassium carbonate yields the 1-aryl-5-oxo-Δ2-pyrrolin-3-carbonitriles 2, in presence of triethylamine the 4,6-diamino-1-aryl-2-oxo-2,3-dihydropyrrolopyridin-5-ca
