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6-iodo-2-methyl-3-phenyl-4(3H)-quinazolinone is a complex organic compound belonging to the quinazolinone family, characterized by a quinazolinone core structure with a 6-iodo, 2-methyl, and 3-phenyl substitution pattern. This molecule features a fused bicyclic ring system, with one of the rings being a six-membered quinazolinone ring and the other being a five-membered ring. The 6-iodo group introduces a halogen atom at the 6th position, while the 2-methyl group adds a methyl substituent at the 2nd position. The 3-phenyl group attaches a phenyl ring to the 3rd position, further enhancing the molecular complexity. 6-iodo-2-methyl-3-phenyl-4(3H)-quinazolinone has potential applications in medicinal chemistry, particularly in the development of new drugs, due to its unique structure and properties.

4449-71-2

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4449-71-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4449-71-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,4,4 and 9 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 4449-71:
(6*4)+(5*4)+(4*4)+(3*9)+(2*7)+(1*1)=102
102 % 10 = 2
So 4449-71-2 is a valid CAS Registry Number.
InChI:InChI=1/C15H11IN2O/c1-10-17-14-8-7-11(16)9-13(14)15(19)18(10)12-5-3-2-4-6-12/h2-9H,1H3

4449-71-2Relevant academic research and scientific papers

Synthesis and anti-inflammatory, analgesic, ulcerogenic and cyclooxygenase activities of novel quinazolinyl-Δ2-pyrazolines

Kumar, Ashok,Sharma, Shalabh,Bajaj, Kiran,Bansal, Deepti,Sharma, Shipra,Saxena, Archana K. K.,Lata,Gupta,Srivastava

, p. 1979 - 1984 (2007/10/03)

Synthesis of 2-(ω -chloroacetonyl)-3-substituted-phenyl-6-halo/6,8-dihaloquinazolin-4(3H)-ones 6-10, 2-(ω -hydrazinoacetonyl)-3-substituted-phenyl-6-halo/6,8-dihaloquinazolin-4(3H)ones 11-15 and 1′ -[3H-3-substituted-phenyl-4-oxo-6-halo/6,8-dihaloquinazolin-2-acetonyl] -3′-aryl-5′-(2-substituted-indol-3-yl)-Δ 2-pyrazolines 16-30 have been described. All the compounds have been tested in vivo for their anti-inflammatory, analgesic, ulcerogenic activities and acute toxicity.

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