128094-31-5

Basic information

• Product Name: 3-phenyl-5-styryl-4,5-dihydroisoxazole
• Synonyms: 3-phenyl-5-styryl-4,5-dihydroisoxazole
• CAS NO: 128094-31-5
• Molecular Weight: 249.312
• Mol File: 128094-31-5.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 3-phenyl-5-styryl-4,5-dihydroisoxazole(CAS DataBase Reference)
• NIST Chemistry Reference: 3-phenyl-5-styryl-4,5-dihydroisoxazole(128094-31-5)
• EPA Substance Registry System: 3-phenyl-5-styryl-4,5-dihydroisoxazole(128094-31-5)

Safety Data

• Hazardous Substances Data: 128094-31-5(Hazardous Substances Data)

Upstream product

• 873-67-6 benzonitrile oxide 
• 16939-57-4 (E)-buta-1,3-dienylbenzene 
• 614-57-3 1,5-diphenylpenta-2,4-dien-1-one 
• 98-86-2 acetophenone 
• 87831-12-7 (E)-3-hydroxy-1,5-diphenyl-pent-4-en-1-one 
• 104-55-2 3-phenyl-propenal 
• 613-91-2 acetophenone oxime 
• 128094-22-4 (E)-3-Hydroxy-1,5-diphenyl-pent-4-en-1-one oxime 

Downstream Products

• 4872-58-6 3-phenyl-4,5-dihydroisoxazole-5-carboxylic acid 

Relevant articles and documents

Synthesis of 5-Vinyl-2-isoxazolines by Palladium-Catalyzed Intramolecular O-Allylation of Ketoximes

An efficient method for the synthesis of 5-vinyl-2-isoxazolines by Pd-catalyzed intramolecular O-allylation of ketoximes has been developed. The reaction involves Pd(0)-catalyzed π-allyl formation via leaving group ionization or Pd(II)-catalyzed allylic C-H activation followed by intramolecular nucleophilic oxime oxygen attack. This methodology has been elaborated to various value-added products by epoxidation, Wacker oxidation, cross-metathesis, hydroboration-oxidation, dihydroxylation, and catalytic hydrogenation.

Anti-corrosive property of bioinspired environmental benign imidazole and isoxazoline heterocyclics: A cumulative studies of experimental and DFT methods

In the present study, four imidazoline (IDZ) and four isoxazolines (ISO) heterocyclics differing in the nature of methoxy (-OCH3) and aromatic (phenyl and naphthyl) moieties are synthesized, characterized and evaluated as corrosion inhibitors for mild steel in acidic solution of 1 M HCl. Results showed that imidazoline based heterocyclic compounds are better corrosion inhibitors than isoxazoline based heterocyclics and both classes of compounds showed inhibition efficiency of more than 85% at 20 mgL?1 concentration. Results further showed that inhibitors containing methoxy, phenyl, and naphthyl moieties showed higher protection efficiency as compared to the inhibitors without these moieties. PDP Study revealed that investigated IDZs and ISOs acted as mixed type inhibitors and their adsorption on the metallic surface followed the Langmuir adsorption isotherm model. All the experimental results were corroborated by density function theory (DFT) based quantum chemical calculations. Numerous DFT based indices calculated for neutral as well as protonated forms of the IDZs and ISOs in order to get better insight about metal-IDZs/ISOs interactions. Outcomes of the DFT analysis showed that protonated (cationic) form of the all the inhibitors are more strongly adsorbed on the metallic surface as compared to their neutral form.

Reaction of Cα,O-Dilithiooximes with Functionalized Carbonyl Compounds. Part 2. Reaction with α-Chloroketones and α,β-Unsaturated Aldehydes and Ketones

The reaction of Cα,O-Dilithiooximes 2 and α-chloroketones afforded 5-(hydroxymethyl)-Δ2-isoxazolines 4. α,β-Unsaturated aldehydes and ketones reacted with 2 to give the corresponding acyclic 1,2-addition products 5.The latter were cyclized with phosphorus pentoxide to 5-vinyl-Δ2-isoxazolines 6.