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CAS

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1154739-79-3

(S)-3-(4-bromo-3-methylphenyl)-5-(3,5-dichlorophenyl)-5-(trifluoromethyl)-4,5-dihydroisoxazole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1154739-79-3 Structure

  • Basic information

    1. Product Name: (S)-3-(4-bromo-3-methylphenyl)-5-(3,5-dichlorophenyl)-5-(trifluoromethyl)-4,5-dihydroisoxazole
    2. Synonyms:
    3. CAS NO:1154739-79-3
    4. Molecular Formula:
    5. Molecular Weight: 453.086
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1154739-79-3.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: (S)-3-(4-bromo-3-methylphenyl)-5-(3,5-dichlorophenyl)-5-(trifluoromethyl)-4,5-dihydroisoxazole(CAS DataBase Reference)
    10. NIST Chemistry Reference: (S)-3-(4-bromo-3-methylphenyl)-5-(3,5-dichlorophenyl)-5-(trifluoromethyl)-4,5-dihydroisoxazole(1154739-79-3)
    11. EPA Substance Registry System: (S)-3-(4-bromo-3-methylphenyl)-5-(3,5-dichlorophenyl)-5-(trifluoromethyl)-4,5-dihydroisoxazole(1154739-79-3)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 1154739-79-3(Hazardous Substances Data)

1154739-79-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1154739-79-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,5,4,7,3 and 9 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1154739-79:
(9*1)+(8*1)+(7*5)+(6*4)+(5*7)+(4*3)+(3*9)+(2*7)+(1*9)=173
173 % 10 = 3
So 1154739-79-3 is a valid CAS Registry Number.

1154739-79-3Downstream Products

1154739-79-3Relevant articles and documents

AgF-mediated fluorinative cross-coupling of two olefins: Facile access to α-CF3 alkenes and β-CF3 ketones

Gao, Bing,Zhao, Yanchuan,Hu, Jinbo

, p. 638 - 642 (2015)

A AgF-mediated fluorination with a concomitant cross-coupling between a gem-difluoroolefin and a non-fluorinated olefin is reported. This highly efficient method provides facile access to both α-CF3 alkenes and β-CF3 ketones, which otherwise remain challenging to be directly prepared. The application of this method is further demonstrated by the synthesis of bioactive isoxazoline derivatives. This approach represents a conceptually novel route to trifluoromethylated compounds that combines the in situ generation of the CF3 moiety and a C-H functionalization in a single reaction system.

Enantioselective synthesis of trifluoromethyl-substituted 2-isoxazolines: Asymmetric hydroxylamine/enone cascade reaction

Matoba, Kazutaka,Kawai, Hiroyuki,Furukawa, Tatsuya,Kusuda, Akihiro,Tokunaga, Etsuko,Nakamura, Shuichi,Shiro, Motoo,Shibata, Norio

supporting information; experimental part, p. 5762 - 5766 (2010/11/03)

(Figure Presented) Cuts both ways: The title reaction consists of an addition/cyclization/dehydration sequence and affords the biologically important chiral 3,5-diaryl-5-(trifluoromethyl)-2-isoxazolines 1 in excellent yields with high ee values. The flexi

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