1618-64-0 Usage
Chemical class
Benzoxazine derivatives
Explanation
Different sources of media describe the Explanation of 1618-64-0 differently. You can refer to the following data:
1. The compound belongs to a group of chemical compounds derived from benzoxazine, which is a fused ring system consisting of a benzene ring and an oxazine ring.
2. The compound features a trifluoromethyl (-CF3) group, which is a methyl group with three fluorine atoms replacing its hydrogen atoms, attached to a phenyl ring.
3. The central structure of the compound consists of a 1,3-benzoxazine ring system with two oxygen atoms (O) at the 2nd and 4th positions, forming a dioxo group.
4. Due to its unique structure and properties, the compound can be used in the development of new drugs, pesticides, and advanced materials in various industries.
5. The compound's structure makes it a valuable building block for creating new chemical entities through further chemical transformations and developments.
6. The presence of the trifluoromethyl group in the compound contributes to its distinct chemical and physical properties, making it an interesting candidate for research and development in various fields.
Trifluoromethyl group
Attached to a phenyl ring
Core structure
2,4-dioxo-1,3-benzoxazine
Potential applications
Pharmaceuticals, agrochemicals, and materials science
Synthesis
Useful in the synthesis of new compounds
Chemical and physical properties
Influenced by the trifluoromethyl group
Check Digit Verification of cas no
The CAS Registry Mumber 1618-64-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,6,1 and 8 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1618-64:
(6*1)+(5*6)+(4*1)+(3*8)+(2*6)+(1*4)=80
80 % 10 = 0
So 1618-64-0 is a valid CAS Registry Number.
1618-64-0Relevant articles and documents
Synthesis and antiinflammatory activity of certain new 1,2,3-triaryl-2,3-dihydro-4(1H)-quinazolinones
Gineinah,Abdelal,Nasr,Said
, p. 17 - 28 (2007/10/02)
A series of 1,2,3-triaryl-2,3-dihydro-4(1H)-quinazolinones, 4a-e, 5a-e, 6a-e, 7a-e, 8a-d and 9a-d was prepared. The structures of the prepared compound were established from their analytical data, IR spectra, 1H-NMR and mass spectroscopy. Compounds 4a, 4b, 4c, 5b, 5c, 5d, 6a, 6b, 6d, 7a, 7b, 7c, 8a, 8b, 8c, 9a and 9b were tested for antiinflammatory activity in the rat paw edema test. The results revealed that compounds 9b, 9a, 7a and 7b produced significant antiinflammatory activity at a dose of 100 mg/kg, i.e., about 30-70% inhibition of edema. Whereas, flufenamic acid at a dose of 10 mg/kg caused 70% inhibition.
