23088-52-0 Usage
Uses
Used in Pharmaceutical Industry:
5-Phenyl-3-isoxazolecarboxamide is used as a chemical building block for the synthesis of various pharmaceuticals. Its antiproliferative and antitumor properties make it a promising candidate for the development of new drugs to treat cancer.
Used in Agrochemical Industry:
5-Phenyl-3-isoxazolecarboxamide is also used as a chemical building block in the synthesis of agrochemicals. Its potential applications in this industry may include the development of new pesticides or herbicides.
Used in Anti-inflammatory and Analgesic Applications:
Due to its potential as an anti-inflammatory and analgesic agent, 5-Phenyl-3-isoxazolecarboxamide is used in the development of medications aimed at reducing inflammation and pain.
Used in Neuroprotective and Anticonvulsant Applications:
5-Phenyl-3-isoxazolecarboxamide is used in the research and development of neuroprotective agents and anticonvulsant drugs, targeting conditions such as epilepsy and other neurological disorders.
Check Digit Verification of cas no
The CAS Registry Mumber 23088-52-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,0,8 and 8 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 23088-52:
(7*2)+(6*3)+(5*0)+(4*8)+(3*8)+(2*5)+(1*2)=100
100 % 10 = 0
So 23088-52-0 is a valid CAS Registry Number.
InChI:InChI=1/C10H8N2O2/c11-10(13)8-6-9(14-12-8)7-4-2-1-3-5-7/h1-6H,(H2,11,13)
23088-52-0Relevant academic research and scientific papers
Synthesis and antimicrobial evaluation of new isoxazole carboxamides
Lavanya,Narayan Reddy,Saritha Jyostna,Ramsubba Reddy
, p. 279 - 280 (2013/09/24)
A new series of 5-phenyl-3-isoxazole carboxamides (4a-j) have been synthesized by reacting 5-phenyl-3-isoxazole carboxylate with various amines. All the synthesized compounds were characterized by their analytical and spectral data. These compounds were-e
Structural Investigation of 3,5-Disubstituted Isoxazoles by 1H-Nuclear Magnetic Resonance
Sechi, Mario,Sannia, Luciano,Orecchioni, Maria,Carta, Fabrizio,Paglietti, Giuseppe,Neamati, Nouri
, p. 1097 - 1102 (2007/10/03)
HIV-1 integrase (IN) is a very promising and validated target for the development of therapeutic agents against AIDS. In an effort to design and synthesize biological isosteric analogs of β-diketoacid-containing inhibitors of IN, we prepared a series of s
Reaction of 3,4-disubstituted 1,2,5-oxadiazole 2-oxides with dipolarophiles. Substituent and solvent effect on the reaction courses
Shimizu, Tomio,Hayashi, Yoshiyuki,Taniguchi, Takehiro,Teramura, Kazuhiro
, p. 727 - 738 (2007/10/02)
A variety of symmetrically or unsymmetrically 3,4-disubstituttd furoxans such as dicyano, dialkyl, diacyl, bis(phenylsulfonyl), N.N'-dialkyldicarbamoyl, 3(or 4)-methyl-4(or -3)-phenyl(or nitro, ethoxy, phenoxy, phenylthio, pyrrolidinyl, phenylsulfonyl), 3
