293326-06-4 Usage
Properties
1. Chemical Formula: $C14H10N2O4$
2. Molecular Weight: Calculate the molecular weight using the atomic weights of carbon, hydrogen, nitrogen, and oxygen.
3. Structure: It features a 1,3-benzoxazin-4-one ring system with a 3-nitrophenyl group attached at the 2-position.
4. Synthetic Nature: It's a synthetic organic molecule.
5. Versatility: Exhibits potential pharmaceutical and industrial applications.
6. Functional Groups: Contains a nitrophenyl group.
Specific Content
1. 1,3-Benzoxazin-4-one Ring System: Central structural motif.
2. 3-Nitrophenyl Group: Attached at the 2-position of the benzoxazinone ring.
3. Chemical and Physical Properties: Affected by the presence of the nitrophenyl group.
4. Building Block: Utilized in the synthesis of other organic compounds.
5. Starting Material: Used for the production of pharmaceuticals or agrochemicals.
6. Research and Industrial Applications: Due to its unique properties and versatility.
This compound serves as a versatile platform for further chemical modifications and applications in various fields of chemistry and industry, owing to its structural diversity and potential reactivity.
Check Digit Verification of cas no
The CAS Registry Mumber 293326-06-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,9,3,3,2 and 6 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 293326-06:
(8*2)+(7*9)+(6*3)+(5*3)+(4*2)+(3*6)+(2*0)+(1*6)=144
144 % 10 = 4
So 293326-06-4 is a valid CAS Registry Number.
293326-06-4Relevant articles and documents
Synthesis and anticonvulsant activity evaluation of 2-Phenyl-2H-benzo[e][1, 3]oxazin-4(3H)-ones
Cui, Li-Jing,Guo, Jun,Gong, Guo-Hua,Quan, Zhe-Shan
, p. 2553 - 2556 (2014/06/09)
A series of new 2-phenyl-2H-benzo[e][1,3]oxazin-4(3H)-one derivatives (1a-1t) were designed based on the known anticonvulsant activity of quinolinone derivatives. All target compounds 1a-1t, characterized by IR, 1H NMR and MS, have been evaluated for their anticonvulsant activity against MES-induced seizures. The pharmacological results showed that all the compounds displayed some degree of anticonvulsant activity. Among them, 2-phenyl-2,3-dihydrobenzo[e][1,3]oxazin-4-one (1a) and 2-(2-fluorophenyl)-2,3- dihydrobenzo-[e][1,3]oxazin-4- one (1b) were considerd more promising because of their lower ED50 (34.1 and 28.4 mg/kg) and higher protective index (11.1 and 8.0).
