223802-38-8 Usage
Uses
Used in Pharmaceutical Research:
2,4-Azetidinedione, 3-methyl-1-phenylis used as a building block in pharmaceutical research for its potential as an anti-inflammatory and analgesic agent. Its unique structure and properties make it a valuable component in the development of new drugs.
Used in Neurological and Psychiatric Disorders Treatment:
In the field of medicine, 2,4-Azetidinedione, 3-methyl-1-phenylis used as a potential treatment for various neurological and psychiatric disorders. Its specific mechanism of action and therapeutic potential are currently under investigation.
Used in Antimicrobial Applications:
2,4-Azetidinedione, 3-methyl-1-phenylhas been studied for its potential antimicrobial properties, making it a candidate for use in the development of new antibiotics or antimicrobial agents to combat resistant bacteria.
Used in Antitumor Applications:
Furthermore, 2,4-Azetidinedione, 3-methyl-1-phenylhas been investigated for its potential antitumor properties, indicating its possible use in cancer research and the development of novel anticancer drugs.
Check Digit Verification of cas no
The CAS Registry Mumber 223802-38-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,3,8,0 and 2 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 223802-38:
(8*2)+(7*2)+(6*3)+(5*8)+(4*0)+(3*2)+(2*3)+(1*8)=108
108 % 10 = 8
So 223802-38-8 is a valid CAS Registry Number.
223802-38-8Relevant academic research and scientific papers
[2+2] and [2+4] type cycloadditions of isocyanates with ynolates
Shindo, Mitsuru,Harada, Akiko,Matsumoto, Kenji,Shishido, Kozo
, p. 39 - 43 (2007/10/03)
Ynolates react with isocyanates to give azetidine-2,4-diones via a [2+2] type cycloaddition. The [4+2] type cycloaddition proceeds in the reactions of vinyl isocyanates with ynolates to provide 2-pyridones.
The Chemistry of 5-Oxodihydroisoxazoles. Part 23. Photochemical and Thermal Reactions of Isoxazol-5(2H)-ones Substituted at C-3 or C-4 with Nitrogen, Oxygen or Sulfur
Khalafy, Jabbar,Prager, Rolf H.,Smith, Jason A.
, p. 518 - 536 (2007/10/03)
The photolysis of 2,3-dimethyl-4-phenoxy- and 4-thiophenoxyisoxazol-5(2H)-one in methanol has been re-examined, but no new products were isolated. Flash vacuum pyrolysis of the former gave a novel product, phenyl N-methylpropenimidate, from rearrangement of the intermediate carbene. Irradiation of the 3-hydroxy-2-phenyl-4-carboxylate gave two products which arise from the 3-hydroxy and 5-hydroxy tautomers. By contrast, the 3-hydroxy-4-acetyl isoxazolone reacted exclusively as one tautomer giving the expected loss of CO2 to form the carbene which was captured by methanol on photolysis, or underwent methyl migration and cyclisation to 3-methylazetidine-1,3-dione on pyrolysis. 3-Amino and 3-phenylamino substituted isoxazolones also gave photolysis and pyrolysis products characteristic of discrete tautomers.
