37795-69-0 Usage
Uses
Used in Pharmaceutical Industry:
2,3-Dihydro-isoxazolo[3,2b]quinazolin-9-one serves as a key building block in the development of new pharmaceuticals. Its unique structure allows it to be a versatile component in the creation of drugs targeting various diseases and conditions. 2,3-DIHYDRO-ISOXAZOLO[3,2B]QUINAZOLIN-9-ONE's potential therapeutic applications are currently under investigation, with the aim of identifying its efficacy and safety in treating specific health issues.
Used in Medicinal Chemistry Research:
In the realm of medicinal chemistry, 2,3-dihydro-isoxazolo[3,2b]quinazolin-9-one is utilized as a subject of study for its chemical properties and potential interactions with biological systems. Researchers are interested in understanding how 2,3-DIHYDRO-ISOXAZOLO[3,2B]QUINAZOLIN-9-ONE can be modified or combined with other molecules to create new therapeutic agents or improve existing ones. Its role in advancing our knowledge of drug design and development is significant, as it may lead to the discovery of novel treatments and therapies.
Check Digit Verification of cas no
The CAS Registry Mumber 37795-69-0 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, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 37795-69:
(7*3)+(6*7)+(5*7)+(4*9)+(3*5)+(2*6)+(1*9)=170
170 % 10 = 0
So 37795-69-0 is a valid CAS Registry Number.
InChI:InChI=1/C10H8N2O2/c13-10-7-3-1-2-4-8(7)11-9-5-6-14-12(9)10/h1-4H,5-6H2
37795-69-0Relevant academic research and scientific papers
New Reaction of Deoxyvasicinone. Part 6
Dunn, A. D.,Kinnear, K. I.,Norrie, R.,Ringan, N.,Martin, D.
, p. 175 - 180 (2007/10/02)
Several acylated derivatives of deoxyvasicinone 1 and its analogues were shown to exist as enols.The 3-hydroxymethyl derivative of 1 was shown to undergo rapid dehydration and products derived from an intermediate 3-methylene compound were obtained.Novel oxazepino analogues of 1 are reported.
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.
