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5-Methyl-3,4-diphenylisoxazole

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Products Intro: Product Name:5-methyl-3,4-diphenylisoxazole
CAS:37928-17-9
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CAS:37928-17-9
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CAS:37928-17-9
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CAS:37928-17-9
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Products Intro: Product Name:5-Methyl-3,4-diphenylisoxazole
CAS:37928-17-9
Purity:99% Package:1kg;50USD

5-Methyl-3,4-diphenylisoxazole manufacturers

5-Methyl-3,4-diphenylisoxazole Basic information
Product Name:5-Methyl-3,4-diphenylisoxazole
Synonyms:Valdecoxib Impurity 10 (Desulfonamide);4-diphenyl-(Parecoxib sodiuM inteMediate);5-Methyl-3;Parecoxib impurity 5/5-methyl-3,4-diphenylisoxazole;Isoxazole, 5-Methyl-3,4-diphenyl- (Parecoxib sodiuM inteMediate);Isoxazole, 5-Methyl-3,4-diphenyl-;3,4-Diphenyl-5-methylisoxazole;5-Methyl-3,4-diphenylisoxazole
CAS:37928-17-9
MF:C16H13NO
MW:235.28
EINECS:1592732-453-0
Product Categories:API;1
Mol File:37928-17-9.mol
5-Methyl-3,4-diphenylisoxazole Structure
5-Methyl-3,4-diphenylisoxazole Chemical Properties
Melting point 96.0 to 100.0 °C
Boiling point 340.1±21.0 °C(Predicted)
density 1.108±0.06 g/cm3(Predicted)
storage temp. Sealed in dry,Room Temperature
solubility Chloroform (Slightly), DMSO (Slightly), Methanol (Slightly)
form Solid
pka-2.53±0.50(Predicted)
color White to Off-White
InChIInChI=1S/C16H13NO/c1-12-15(13-8-4-2-5-9-13)16(17-18-12)14-10-6-3-7-11-14/h2-11H,1H3
InChIKeyZXIRUKJWLADSJS-UHFFFAOYSA-N
SMILESO1C(C)=C(C2=CC=CC=C2)C(C2=CC=CC=C2)=N1
Safety Information
HS Code 2934.99.4400
MSDS Information
5-Methyl-3,4-diphenylisoxazole Usage And Synthesis
Uses5-Methyl-3,4-diphenylisoxazole is synthesis The key intermediate of Parecoxib Sodium (Parecoxib Sodium).Parecoxib Sodium is by the Pfizer of the U.S. The cox 2 inhibitor of company's research and development, listed in European Union in 2002, trade name Dynastat, is used for The short term therapy of postoperative pain.
Uses5-Methyl-3,4-diphenylisoxazole is a reagent for the preparation of valdecoxib and valdecoxib analogues.
SynthesisSynthesis_37928-17-9
In four mouthfuls of round-bottomed flasks of a 1L add compound 2 (40g), methanol (400mL), 7.7% Aqueous sodium carbonate (400mL), is heated to 70°C, after stirring reaction 2h, and TLC plate monitoring raw material Fundamental reaction is complete, and solution is divided into solid-liquid biphase, is extracted with ethyl acetate, collected organic layer, with anhydrous Sodium sulfate is dried, and vacuum obtains white solid, HPLC purity: 94.9% after being spin-dried for.White solid uses 40ml ethyl acetate and the mixed solvent recrystallization of 120ml normal hexane (1:3) again, Obtaining target compound is white solid 34.2g, yield 92%, HPLC purity: 99.7%.m.p.97-98??£? MS(m/z):236(M+H)+£?1H NMR(400MHz,CDCl3) |?:2.43(s,3H,-CH3), 7.19-7.43 (m, 10H ,-CH=).
References[1] Patent: CN105949141, 2016, A. Location in patent: Paragraph 0016; 0021; 0022; 0023; 0025; 0027; 0029-0041
[2] Patent: CN104193694, 2016, B. Location in patent: Paragraph 0029; 0030; 0031
Tag:5-Methyl-3,4-diphenylisoxazole(37928-17-9) Related Product Information
BenzenesulfonaMide, 3-[4-[4-(aMinosulfonyl)phenyl]-5-Methyl-3-isoxazolyl]- Valdecoxib IMpurity B Parecoxib 1-Hydroxy Valdecoxib Parecoxib Impurity 18 Valdecoxib 3'-Sulfonyl Chloride IMpurity 5-Methyl-3-phenyl-4-(phenylMethyl)isoxazole 4-(4-chlorophenyl)-5-methyl-3-phenylisoxazole N-((4-(5-Methyl-3-phenylisoxazol-4-yl)phenyl)sulfonyl)acetaMide 4-[(5-Methyl-3-phenyl-4-isoxazolyl)methyl]benzenesulfonamide 2-Phenylacetophenone 3-methyl -4,5-diphenyl-4,5-didydro-isoxazole Valdecoxib IMpurity-E Valdecoxib Deoxybenzoin Oxime 5-METHYL-3,4-DIPHENYL-4,5-DIHYDROISOXAZOL-5-OL Valdecoxib IMpurity D PARECOXIB SODIUM

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