106595-91-9 Usage
Uses
Used in Pharmaceutical Industry:
4-BENZYL-1,3-DIHYDROQUINOXALIN-2-ONE is used as a building block for the synthesis of bioactive molecules and pharmaceutical intermediates, contributing to the development of new drugs and therapeutic agents.
Used in Organic Synthesis:
In the field of organic synthesis, 4-BENZYL-1,3-DIHYDROQUINOXALIN-2-ONE is used as a key component in the creation of complex organic compounds, facilitating advancements in chemical research and the production of novel materials.
Used in Biological Research:
4-BENZYL-1,3-DIHYDROQUINOXALIN-2-ONE is used as a subject of study for its potential anticonvulsant properties, aiding in the exploration of new treatments for seizure disorders and other related conditions.
Used in Analytical Chemistry:
As a reagent, 4-BENZYL-1,3-DIHYDROQUINOXALIN-2-ONE is used for the determination of mercury and other metals, playing a crucial role in environmental and industrial analyses to ensure safety and compliance with regulations.
Used in Coordination Chemistry:
4-BENZYL-1,3-DIHYDROQUINOXALIN-2-ONE is utilized as a ligand in coordination chemistry, enabling the formation of coordination compounds with potential applications in catalysis, materials science, and other areas of chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 106595-91-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,6,5,9 and 5 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 106595-91:
(8*1)+(7*0)+(6*6)+(5*5)+(4*9)+(3*5)+(2*9)+(1*1)=139
139 % 10 = 9
So 106595-91-9 is a valid CAS Registry Number.
InChI:InChI=1/C15H14N2O/c18-15-11-17(10-12-6-2-1-3-7-12)14-9-5-4-8-13(14)16-15/h1-9H,10-11H2,(H,16,18)
106595-91-9Relevant academic research and scientific papers
Formal Deoxygenative Hydrogenation of Lactams Using PNHP-Pincer Ruthenium Complexes under Nonacidic Conditions
Ogata, Osamu,Nara, Hideki,Matsumura, Kazuhiko,Kayaki, Yoshihito
supporting information, p. 9954 - 9959 (2019/12/24)
A formal deoxygenative hydrogenation of amides to amines with RuCl2(NHC)(PNHP) (NHC = 1,3-dimethylimizadol-2-ylidene, PNHP = bis(2-diphenylphosphinoethyl)amine) is described. Various secondary amides, especially NH-lactams, are reduced with H2 (3.0-5.0 MPa) to amines at a temperature range of 120-150 °C with 1.0-2.0 mol % of PNHP-Ru catalysts in the presence of Cs2CO3. This process consists of (1) deaminative hydrogenation of secondary amides to generate primary amines and alcohols, (2) dehydrogenative coupling of the transient amines with alcohols to generate imines, and (3) hydrogenation of imines to give the formally deoxygenated secondary amine products.
