polymerization inhibitor QM-PH

  • CAS:7078-98-0
  • MF:C21H26 O
  • Purity:99%
  • Molecular Weight:294.437
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Product Details

  • CAS: 7078-98-0
  • MF: C21H26 O
  • Quality manufacturer supply polymerization inhibitor QM-PH 7078-98-0 in stock with high standard

    • Molecular Formula:C21H26 O
    • Molecular Weight:294.437
    • Vapor Pressure:1.82E-07mmHg at 25°C 
    • Melting Point:74-75 °C 
    • Boiling Point:426.1°C at 760 mmHg 
    • Flash Point:183°C 
    • PSA:17.07000 
    • Density:1.03g/cm3 
    • LogP:5.59770 

    2,6-BIS(1,1-DIMETHYLETHYL)-4-(PHENYLMETHYLENE)-2,5-CYCLOHEXADIEN-1-ONE(Cas 7078-98-0) Usage

    Flammability and Explosibility

    Nonflammable

    InChI:InChI=1/C21H26O/c1-20(2,3)17-13-16(12-15-10-8-7-9-11-15)14-18(19(17)22)21(4,5)6/h7-14H,1-6H3

    7078-98-0 Relevant articles

    Isothiourea-catalyzed enantioselective α-alkylation of esters via 1,6-conjugate addition to para-quinone methides

    Arokianathar, Jude N.,Greenhalgh, Mark D.,Hartley, Will C.,McLaughlin, Calum,Ng, Sean,Slawin, Alexandra M. Z.,Smith, Andrew D.,Stead, Darren

    supporting information, (2021/11/01)

    The isothiourea-catalyzed enantioselecti...

    Preparation method of 4-phenyl methylene-2, 6-di-tert-butyl-2, 5-cyclohexadiene-1-ketone and derivative thereof

    -

    Paragraph 0036-0047, (2021/05/05)

    The invention provides a preparation met...

    Vinylogous Aza-Michael Addition of Urea Derivatives with p-Quinone Methides Followed by Oxidative Dearomative Cyclization: Approach to Spiroimidazolidinone Derivatives

    Kaur, Navpreet,Singh, Priyanka,Banerjee, Prabal

    supporting information, p. 2813 - 2824 (2021/04/21)

    Herein, we report an efficient protocol ...

    Enantioselective Stetter Reactions Catalyzed by Bis(amino)cyclopropenylidenes: Important Role for Water as an Additive

    Rezazadeh Khalkhali, Mehran,Wilde, Myron M. D.,Gravel, Michel

    supporting information, p. 155 - 159 (2021/01/09)

    The first highly enantioselective interm...

    7078-98-0 Process route

    2,6-di-tert-butylphenol
    128-39-2

    2,6-di-tert-butylphenol

    benzaldehyde
    100-52-7

    benzaldehyde

    2,6-di-tert-butyl-4-benzylidene-cyclohexa-2,5-dienone
    7078-98-0

    2,6-di-tert-butyl-4-benzylidene-cyclohexa-2,5-dienone

    Conditions
    Conditions Yield
    2,6-di-tert-butylphenol; benzaldehyde; With piperidine; In toluene; for 3h; Reflux;
    With acetic anhydride; In toluene; at 110 - 125 ℃; for 0.5h;
    79.1%
    2,6-di-tert-butylphenol; benzaldehyde; With piperidine; In toluene; Reflux;
    With acetic anhydride; In toluene; for 0.25h;
    78%
    2,6-di-tert-butylphenol; benzaldehyde; With piperidine; In toluene; for 19h; Reflux; Dean-Stark;
    With acetic anhydride; In toluene; for 1h; Reflux; Dean-Stark;
    78%
    With piperidine; zinc(II) chloride; In toluene; Reagent/catalyst; Reflux; Dean-Stark;
    77.39%
    2,6-di-tert-butylphenol; benzaldehyde; With piperidine; In toluene; for 7h; Dean-Stark; Reflux; Inert atmosphere;
    With acetic anhydride; In toluene; Dean-Stark; Heating; Inert atmosphere;
    76%
    2,6-di-tert-butylphenol; benzaldehyde; With piperidine; In toluene; for 13h; Dean-Stark; Reflux;
    With acetic anhydride; In toluene; for 0.25h; Dean-Stark;
    74%
    2,6-di-tert-butylphenol; benzaldehyde; With piperidine; In toluene; for 13h; Reflux; Dean-Stark;
    With acetic anhydride; In toluene; at 100 ℃; for 1h;
    70%
    2,6-di-tert-butylphenol; benzaldehyde; With piperidine; In toluene; for 3h; Dean-Stark; Reflux; Inert atmosphere;
    With acetic anhydride; In toluene; for 0.25h; Heating; Inert atmosphere;
    69%
    2,6-di-tert-butylphenol; benzaldehyde; With piperidine; In toluene; at 110 ℃; for 12h; Dean-Stark;
    With acetic anhydride; In toluene; at 100 ℃; for 0.5h;
    52%
    With piperidine; In toluene; for 13h; Inert atmosphere; Reflux; Dean-Stark;
    32%
    With piperidine; In butan-1-ol; for 24h; Reflux;
    2,6-di-tert-butylphenol; benzaldehyde; In toluene; for 4h; Dean-Stark; Reflux; Alkaline conditions;
    With acetic anhydride; In toluene; for 0.25h; Dean-Stark;
    With piperidine; In toluene; for 4h; Dean-Stark; Reflux;
    2,6-di-tert-butylphenol; benzaldehyde; With piperidine; In toluene; at 140 ℃; for 13h; Dean-Stark; Inert atmosphere; Heating;
    With acetic anhydride; In toluene; for 0.25h; Dean-Stark; Inert atmosphere; Heating;
    With pyridine; acetic anhydride; In toluene; for 4h; Reflux; Dean-Stark;
    2,6-di-tert-butylphenol; benzaldehyde; In toluene; for 1h; Reflux; Inert atmosphere; Dean-Stark;
    With piperidine; In toluene; for 5h; Reflux; Inert atmosphere; Dean-Stark;
    With piperidine; In toluene; for 4h; Dean-Stark; Reflux;
    2,6-di-tert-butylphenol; benzaldehyde; With piperidine; In toluene; for 4h; Dean-Stark; Reflux;
    With acetic anhydride; In toluene; for 0.25h;
    2,6-di-tert-butylphenol; benzaldehyde; With piperidine; In toluene; for 4h; Reflux;
    With acetic anhydride; In toluene; at 20 ℃; for 0.25h;
    2,6-di-tert-butylphenol; benzaldehyde; With piperidine; In toluene; for 3h; Reflux; Dean-Stark;
    With acetic anhydride; In toluene; for 0.25h; Heating;
    2,6-di-tert-butylphenol; benzaldehyde; In toluene; for 1h; Reflux; Dean-Stark;
    With piperidine; In toluene; for 3h; Reflux; Dean-Stark;
    With acetic anhydride; In toluene; for 0.25h;
    2,6-di-tert-butylphenol; benzaldehyde; With piperidine; In toluene; for 24h; Reflux;
    With acetic anhydride; In toluene; for 0.25h;
    Multi-step reaction with 2 steps
    1: 0.5 h / 120 °C / Microwave irradiation
    2: acetic anhydride / 0.05 h / 120 °C / Microwave irradiation; Green chemistry
    With acetic anhydride; 1: |Mannich Aminomethylation;
    2,6-di-tert-butylphenol; benzaldehyde; With di-n-propylamine; In toluene; Dean-Stark; Reflux;
    With acetic anhydride; In toluene; for 0.25h;
    2,6-di-tert-butylphenol; benzaldehyde; With piperidine; In toluene; Dean-Stark; Reflux;
    With acetic anhydride; In toluene; for 0.5h; Dean-Stark; Reflux;
    2,6-di-tert-butylphenol; benzaldehyde; With piperidine; In toluene; for 12h; Reflux; Inert atmosphere;
    With acetic anhydride; In toluene; for 0.25h; Inert atmosphere;
    2,6-di-tert-butylphenol; benzaldehyde; In toluene; Reflux;
    With piperidine; In toluene; Reflux;
    With acetic anhydride; In toluene; for 0.25h;
    With piperidine; In toluene; at 150 ℃; Dean-Stark;
    2,6-di-tert-butylphenol; benzaldehyde; With piperidine; In toluene; at 110 ℃;
    With acetic anhydride; In toluene; for 0.25h; Reflux;
    2,6-di-tert-butylphenol; benzaldehyde; In toluene; for 4h; Dean-Stark; Reflux;
    With acetic anhydride; In toluene; for 0.25h; Dean-Stark;
    With piperidine; In toluene; for 12h; Dean-Stark; Reflux;
    2,6-di-tert-butylphenol; benzaldehyde; With piperidine; In toluene; for 4h; Dean-Stark; Reflux;
    With acetic anhydride; In toluene; for 0.25h; Dean-Stark;
    2,6-di-tert-butylphenol; benzaldehyde; With piperidine; In toluene; Dean-Stark; Reflux;
    With acetic anhydride; In toluene; for 0.5h; Reflux; Dean-Stark;
    2,6-di-tert-butylphenol; benzaldehyde; With piperidine; In toluene; Dean-Stark; Reflux;
    With acetic anhydride; In toluene; for 0.5h; Dean-Stark;
    2,6-di-tert-butylphenol; benzaldehyde; With piperidine; In toluene; at 140 ℃; Dean-Stark;
    With acetic anhydride; In toluene; for 0.25h; Dean-Stark; Heating;
    2,6-di-tert-butylphenol; benzaldehyde; With pyrrolidine; In toluene; at 110 ℃; for 3h;
    With butanoic acid anhydride; In toluene; for 1h;
    With piperidine; In toluene; at 120 ℃; for 12h;
    2,6-di-tert-butylphenol; benzaldehyde; With piperidine; In toluene; for 13h; Reflux;
    With acetic anhydride; In toluene; for 0.25h;
    2,6-di-tert-butylphenol; benzaldehyde; With piperidine; In toluene; for 6h; Heating; Reflux;
    With acetic anhydride; for 0.5h;
    2,6-di-tert-butylphenol; benzaldehyde; With piperidine; In toluene; at 140 ℃; for 1h; Dean-Stark;
    With acetic anhydride; In toluene; for 0.25h; Dean-Stark;
    2,6-di-<i>tert</i>-butyl-4-(phenyl-piperidin-1-yl-methyl)-phenol
    17330-09-5

    2,6-di-tert-butyl-4-(phenyl-piperidin-1-yl-methyl)-phenol

    2,6-di-tert-butyl-4-benzylidene-cyclohexa-2,5-dienone
    7078-98-0

    2,6-di-tert-butyl-4-benzylidene-cyclohexa-2,5-dienone

    Conditions
    Conditions Yield
    With acetic anhydride; at 120 ℃; for 0.05h; Microwave irradiation; Green chemistry;
    70.18%

    7078-98-0 Upstream products

    • 4973-27-7
      4973-27-7

      4-benzyl-2,6-di-tert-butylphenol

    • 20017-39-4
      20017-39-4

      (3,5-di-tert-butyl-4-hydroxyphenyl)phenylcarbinol

    • 591-51-5
      591-51-5

      phenyllithium

    • 1620-98-0
      1620-98-0

      3,5-di-t-butyl-4-hydroxybenzaldehyde

    7078-98-0 Downstream products

    • 719-22-2
      719-22-2

      2,6-Di-tert-butyl-1,4-benzoquinone

    • 77488-14-3
      77488-14-3

      5,7-Di-tert-butyl-2-phenyl-1-oxa-spiro[2.5]octa-4,7-dien-6-one

    • 100-52-7
      100-52-7

      benzaldehyde

    • 96275-07-9
      96275-07-9

      4-((benzyloxy)(phenyl)methyl)-2,6-di-tert-butylphenol

    Antioxidant BHT 264

    CAS:128-37-0

    Purity:99%

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