7471-58-1 Usage
Uses
Used in Pharmaceutical Industry:
2(1H)-Quinazolinone (6CI,8CI,9CI) is used as a key intermediate in the synthesis of pharmaceuticals for its diverse pharmacological properties. It serves as a building block for developing new drugs with potential applications in treating various diseases, including cancer, inflammation, and viral infections.
Used in Organic Synthesis:
In the field of organic synthesis, 2(1H)-Quinazolinone (6CI,8CI,9CI) is utilized as a versatile starting material for the creation of a wide range of organic compounds. Its unique structure allows for the formation of various derivatives, expanding the scope of chemical research and development.
Used in Neurological Disorder Treatment:
2(1H)-Quinazolinone (6CI,8CI,9CI) is being studied for its potential application in the treatment of neurological disorders. Its pharmacological profile suggests that it may have neuroprotective effects, making it a candidate for further research and development in this area.
Used as an Anti-Depressant:
2(1H)-Quinazolinone (6CI,8CI,9CI) is also being explored for its potential as an anti-depressant. Its ability to modulate mood and potentially alleviate symptoms of depression positions it as a candidate for further investigation in the field of mental health.
Overall, 2(1H)-Quinazolinone (6CI,8CI,9CI) is a multifaceted chemical with applications spanning across various industries, particularly in pharmaceuticals and organic synthesis, and holds promise for future therapeutic developments.
Check Digit Verification of cas no
The CAS Registry Mumber 7471-58-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,4,7 and 1 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 7471-58:
(6*7)+(5*4)+(4*7)+(3*1)+(2*5)+(1*8)=111
111 % 10 = 1
So 7471-58-1 is a valid CAS Registry Number.
InChI:InChI=1/C8H6N2O/c11-8-9-5-6-3-1-2-4-7(6)10-8/h1-5H,(H,9,10,11)
7471-58-1Relevant academic research and scientific papers
Enzymatic analysis using substrates that yield fluorescent precipitates
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, (2008/06/13)
Novel fluorescent precipitating substrates made from a class of fluorophores, generally including quinazolinones (quinazolones), benzimidazoles, benzothiazoles, benzoxazoles, quinolines, indolines, and phenanthridines, having the general formula: STR1 where carbon atoms of --C1 =C2 -- are further joined so as to complete a first 5- or 6-membered aromatic ring which may contain at least one of the hetero atoms N, O or S, where carbon atoms of --C4 --N=C3 -- are further joined so as to complete a second 5- or 6-membered aromatic ring that contains at least the nitrogen between C3 and C4 and may contain at least one additional hetero atom N, O or S, where the first and second aromatic rings may be joined by a 5- or 6-membered bridging ring that contains at least the C2 from the first aromatic ring and the C3 from the second aromatic ring, which bridging ring may be saturated or unsaturated and may contain a hetero atom N, O, or S, where each of the first and second aromatic rings may be fused to at least one additional aromatic ring that may contain at least one of the hetero atoms N, O or S, and where each of said aromatic rings may be further modified by substitution of any hydrogens on an aromatic carbon by substituents that are halogen, nitro, cyano, aryl, lower alkyl (1-4 carbons), perfluoroalkyl (1-4 carbons), or alkoxy (1-4 carbons), or any combination thereof; and Xfl is covalently linked to the oxygen --O-- at C1.
