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14441-90-8

  • Product Name:5-PHENYLISOXAZOLE-3-CARBOXYLIC ACID
  • Molecular Formula:C10H7NO3
  • Purity:99%
  • Molecular Weight:189.17
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Product Details

  • CasNo: 14441-90-8
  • Molecular Formula: C10H7NO3
  • Buy Reliable Quality Best Quality 5-PHENYLISOXAZOLE-3-CARBOXYLIC ACID 14441-90-8 Cheap Price

    • Molecular Formula:C10H7NO3
    • Molecular Weight:189.17
    • Vapor Pressure:2.51E-08mmHg at 25°C 
    • Melting Point:160-164 °C(lit.) 
    • Boiling Point:434.7 °C at 760 mmHg 
    • PKA:3.33±0.10(Predicted) 
    • Flash Point:216.7 °C 
    • PSA:63.33000 
    • Density:1.32 g/cm3 
    • LogP:2.03980 

    5-PHENYLISOXAZOLE-3-CARBOXYLIC ACID(Cas 14441-90-8) Usage

    5-Phenylisoxazole-3-carboxylic acid has been shown to inhibit the growth of tuberculosis bacteria. Some derivatives of 5-phenylisoxazole-3-carboxylic acid have been synthesized and analyzed for their ability to inhibit xanthine oxidase.

    InChI:InChI=1/C10H7NO3/c12-10(13)8-6-9(14-11-8)7-4-2-1-3-5-7/h1-6H,(H,12,13)/p-1

    14441-90-8 Relevant articles

    Synthesis of some 5-phenylisoxazole-3-carboxylic acid derivatives as potent xanthine oxidase inhibitors

    Shaojie Wang a, Jufang Yan b, Jian Wang a, Jiarun Chen a, Tingjian Zhang a, Yong Zhao a, Mingxing Xue a

    , European Journal of Medicinal Chemistry Volume 45, Issue 6, June 2010, Pages 2663-2670

    A number of 5-phenylisoxazole-3-carboxylic acid derivatives (5a–e, 11a–e) were synthesized and analyzed for their ability to inhibit xanthine oxidase. Most of the compounds exhibited potency levels in the micromolar/submicromolar range.

    Synthesis and in Vitro Cytotoxic Activity of Novel Triazole-Isoxazole Derivatives

    Najafi, Zahra,Mahdavi, Mohammad,Safavi, Maliheh,Saeedi, Mina,Alinezhad, Heshmatollah,Pordeli, Mahboobeh,Kabudanian Ardestani, Sussan,Shafiee, Abbas,Foroumadi, Alireza,Akbarzadeh, Tahmineh

    , p. 1743 - 1747 (2015)

    New derivatives of triazole-isoxazole we...

    Design, synthesis, and biological activity evaluation of 2-(benzo[b]thiophen-2-yl)-4-phenyl-4,5-dihydrooxazole derivatives as broad-spectrum antifungal agents

    Zhao, Liyu,Sun, Yin,Yin, Wenbo,Tian, Linfeng,Sun, Nannan,Zheng, Yang,Zhang, Chu,Zhao, Shizhen,Su, Xin,Zhao, Dongmei,Cheng, Maosheng

    , (2021/11/22)

    To discover antifungal compounds with br...

    Novel N-benzylpiperidine derivatives of 5-arylisoxazole-3-carboxamides as anti-Alzheimer's agents

    Saeedi, Mina,Felegari, Peyman,Iraji, Aida,Hariri, Roshanak,Rastegari, Arezoo,Mirfazli, S. Sara,Edraki, Najmeh,Firuzi, Omidreza,Mahdavi, Mohammad,Akbarzadeh, Tahmineh

    , (2020/11/30)

    The complex pathophysiology of Alzheimer...

    Mechanochemistry Enabled Construction of Isoxazole Skeleton via CuO Nanoparticles Catalyzed Intermolecular Dehydrohalogenative Annulation

    Vadivelu, Murugan,Sampath, Sugirdha,Muthu, Kesavan,Karthikeyan, Kesavan,Praveen, Chandrasekar

    , p. 4941 - 4952 (2021/09/09)

    A dehydrohalogenative approach for isoxa...

    14441-90-8 Process route

    (E)-5-phenyl-3-(2-phenylethenyl)-2-isoxazoline
    107487-07-0

    (E)-5-phenyl-3-(2-phenylethenyl)-2-isoxazoline

    5-phenyl-3-isoxazolecarboxylic acid
    14441-90-8

    5-phenyl-3-isoxazolecarboxylic acid

    benzoic acid
    65-85-0,8013-63-6

    benzoic acid

    Conditions
    Conditions Yield
    (E)-5-phenyl-3-(2-phenylethenyl)-2-isoxazoline; With tert.-butylhydroperoxide; iron(III) chloride hexahydrate; In water; for 1h; Sealed tube;
    With water; sodium hydroxide; at 80 ℃; for 10h; Sealed tube;
     
    (1E,4E)-1,5-diphenylpenta-1,4-dien-3-one oxime
    6502-37-0

    (1E,4E)-1,5-diphenylpenta-1,4-dien-3-one oxime

    5-phenyl-3-isoxazolecarboxylic acid
    14441-90-8

    5-phenyl-3-isoxazolecarboxylic acid

    benzoic acid
    65-85-0,8013-63-6

    benzoic acid

    Conditions
    Conditions Yield
    Multi-step reaction with 3 steps
    1.1: copper diacetate; sodium sulfate; pyridine / 1,2-dichloro-ethane / 12 h / 25 °C
    2.1: iron(III) chloride hexahydrate; 1,10-Phenanthroline / tetrahydrofuran / 80 °C / Inert atmosphere; Sealed tube
    3.1: tert.-butylhydroperoxide; iron(III) chloride hexahydrate / water / 1 h / Sealed tube
    3.2: 10 h / 80 °C / Sealed tube
    With pyridine; tert.-butylhydroperoxide; 1,10-Phenanthroline; iron(III) chloride hexahydrate; copper diacetate; sodium sulfate; In tetrahydrofuran; water; 1,2-dichloro-ethane;
     
    Multi-step reaction with 3 steps
    1.1: copper diacetate; sodium sulfate; pyridine / 1,2-dichloro-ethane / 12 h / 25 °C
    2.1: iron(III) chloride hexahydrate; 1,10-Phenanthroline / tetrahydrofuran / 80 °C / Inert atmosphere; Sealed tube
    3.1: tert.-butylhydroperoxide; iron(III) chloride hexahydrate / water / 1 h / Sealed tube
    3.2: 10 h / 80 °C / Sealed tube
    With pyridine; tert.-butylhydroperoxide; 1,10-Phenanthroline; iron(III) chloride hexahydrate; copper diacetate; sodium sulfate; In tetrahydrofuran; water; 1,2-dichloro-ethane;
     
    Multi-step reaction with 3 steps
    1.1: copper diacetate; sodium sulfate; pyridine / 1,2-dichloro-ethane / 12 h / 25 °C
    2.1: iron(III) chloride hexahydrate; 1,10-Phenanthroline / tetrahydrofuran / 80 °C / Inert atmosphere; Sealed tube
    3.1: tert.-butylhydroperoxide; iron(III) chloride hexahydrate / water / 1 h / Sealed tube
    3.2: 10 h / 80 °C / Sealed tube
    With pyridine; tert.-butylhydroperoxide; 1,10-Phenanthroline; iron(III) chloride hexahydrate; copper diacetate; sodium sulfate; In tetrahydrofuran; water; 1,2-dichloro-ethane;
     
    Multi-step reaction with 3 steps
    1.1: copper diacetate; sodium sulfate; pyridine / 1,2-dichloro-ethane / 12 h / 25 °C
    2.1: iron(III) chloride hexahydrate; 1,10-Phenanthroline / acetonitrile / 80 °C / Inert atmosphere; Sealed tube
    3.1: tert.-butylhydroperoxide; iron(III) chloride hexahydrate / water / 1 h / Sealed tube
    3.2: 10 h / 80 °C / Sealed tube
    With pyridine; tert.-butylhydroperoxide; 1,10-Phenanthroline; iron(III) chloride hexahydrate; copper diacetate; sodium sulfate; In water; 1,2-dichloro-ethane; acetonitrile;
     
    Multi-step reaction with 3 steps
    1.1: copper diacetate; sodium sulfate; pyridine / 1,2-dichloro-ethane / 12 h / 25 °C
    2.1: iron(III) chloride hexahydrate; 1,10-Phenanthroline / tetrahydrofuran / 80 °C
    3.1: tert.-butylhydroperoxide; iron(III) chloride hexahydrate / water / 1 h / Sealed tube
    3.2: 10 h / 80 °C / Sealed tube
    With pyridine; tert.-butylhydroperoxide; 1,10-Phenanthroline; iron(III) chloride hexahydrate; copper diacetate; sodium sulfate; In tetrahydrofuran; water; 1,2-dichloro-ethane;
     

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    Purity:99%

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