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179162-55-1

  • Product Name：4-(5-(4-(pentyloxy)phenyl)isoxazol-3-yl)benzoic acid
  • Molecular Formula：C21H21NO4
  • Purity：99%
  • Molecular Weight：351.402
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Product Details

  • CasNo： 179162-55-1
  • Molecular Formula： C21H21NO4

    • Offer Chinese Manufacturer Supply 4-(5-(4-(pentyloxy)phenyl)isoxazol-3-yl)benzoic acid 179162-55-1 Efficient Transportation

    • Molecular Formula:C21H21NO4
    • Molecular Weight:351.402
    • Melting Point:271-273oC 
    • Boiling Point:555.6±50.0 °C(Predicted) 
    • PKA:3.72±0.10(Predicted) 
    • PSA：72.56000 
    • Density:1.176±0.06 g/cm3(Predicted) 
    • LogP:5.27580 

    179162-55-1 Relevant articles

    FK463, a novel water-soluble echinocandin lipopeptide: Synthesis and antifungal activity [1]

    Tomishima,Ohki,Yamada,Takasugi,Maki,Tawara,Tanaka

    , p. 674 - 676 (1999)

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    Practical synthesis of FR195752, the side chain of Micafungin, utilizing a regioselective conversion of diaryl-β-diketone to 3,5-diarylisoxazole

    Ohigashi, Atsushi,Kanda, Atsushi,Tsuboi, Hiroyuki,Hashimoto, Norio

    , p. 179 - 184 (2005)

    The practical synthesis of FR195752, the...

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    Paragraph 0040; 0042; 0043; 0045, (2020/02/14)

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    supporting information, p. 2180 - 2187 (2019/06/25)

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    Synthesis and antifungal evaluation of pentyloxyl-diphenylisoxazoloyl pneumocandins and echinocandins

    Singh, Sheo B.,Herath, Kithsiri,Kahn, Jennifer Nielsen,Mann, Paul,Abruzzo, George,Motyl, Mary

    , p. 3253 - 3256 (2013/06/27)

    Echinocandins and pneumocandins are clas...

    179162-55-1 Process route

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    Conditions
    Conditions Yield
    Multi-step reaction with 2 steps
    1: 84.5 percent / Et3N / tetrahydrofuran
    2: 97.8 percent / NaOH / ethanol; tetrahydrofuran
    With sodium hydroxide; triethylamine; In tetrahydrofuran; ethanol; 1: Cycloaddition / 2: Hydrolysis;
    		 
    4-methoxycarbonylbenzhydroxamic acid chloride
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    4-methoxycarbonylbenzhydroxamic acid chloride

    4-{5-[4-(pentyloxy)phenyl]-1,2-oxazol-3-yl}benzoic acid
    179162-55-1

    4-{5-[4-(pentyloxy)phenyl]-1,2-oxazol-3-yl}benzoic acid

    Conditions
    Conditions Yield
    Multi-step reaction with 2 steps
    1: 84.5 percent / Et3N / tetrahydrofuran
    2: 97.8 percent / NaOH / ethanol; tetrahydrofuran
    With sodium hydroxide; triethylamine; In tetrahydrofuran; ethanol; 1: Cycloaddition / 2: Hydrolysis;
    		 

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    Antioxidant BHT 264

    CAS:128-37-0

    Purity:99%

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