37795-71-4 Usage
General Description
2,3-dihydro-3-methyl-9H-isoxazolo[3,2-b]quinazolin-9-one is a chemical compound with a complex molecular structure. It is classified as an isoxazoloquinazolinone, which is a type of heterocyclic compound. 2,3-dihydro-3-methyl-9H-isoxazolo[3,2-b]quinazolin-9-one has potential pharmaceutical applications, as it has been studied for its possible anticancer and antiviral properties. Its unique structure may allow for specific interactions with biological targets, making it a promising candidate for further drug development. Additionally, its chemical characteristics make it a valuable tool for researchers studying the structure-activity relationship of similar compounds for medicinal purposes.
Check Digit Verification of cas no
The CAS Registry Mumber 37795-71-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,7,7,9 and 5 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 37795-71:
(7*3)+(6*7)+(5*7)+(4*9)+(3*5)+(2*7)+(1*1)=164
164 % 10 = 4
So 37795-71-4 is a valid CAS Registry Number.
InChI:InChI=1/C11H10N2O2/c1-7-6-15-13-10(7)12-9-5-3-2-4-8(9)11(13)14/h2-5,7H,6H2,1H3
37795-71-4Relevant articles and documents
2,3 Dihydro 9H isoxazolo[3,2 b]quinazolin 9 ones and 3,4 dihydro (1,2) oxazino[3,2 b]quinazolin 10(2H) ones
Reisner,Ludwig,Simon,Dejneka,Sofia
, p. 766 - 770 (2007/10/09)
Two series of compounds, 2,3-dihydro-9H-isoxazolo [3,2-b] quinazolin-9-ones and 3,4-dihydro-(1,2)-oxazino-[3,2-b]quinazolin-10 (2H)-ones, were synthesized and evaluated for anti-inflammatory, antipyretic and analgesic activity. The isoxazolo compounds were generally more active than their oxazino homologs. Three compounds, i.e., 2,3-dihydro 9H isoxazolo [3,2-b]quinazolin-9-one (W-2429) and its 2- and 3-methyl congeners, were the most active of all compounds tested in this study. On the basis of the biological results herein reported, W-2429 is considerably more effective than acetylsalicylic acid in inhibiting carrageenan-induced edema and in reducing brewer's yeast-induced fever in rats. Also, it was found to be more potent than propoxyphene hydrochloride in the Randall-Selitto test for analgesic activity.