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      2-Ethyl anthraquinone (2-EAQ)

      • Product Name: 2-Ethyl anthraquinone (2-EAQ)
      • CAS: 84-51-5
      • Purity:
      • Appearance: white or yellowish crystals or powder

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      Factory supply good quality 2-Ethyl anthraquinone (2-EAQ) 84-51-5 with stock

      • Molecular Formula:C16H12O2
      • Molecular Weight:236.27
      • Appearance/Colour:white or yellowish crystals or powder 
      • Vapor Pressure:4.14E-07mmHg at 25°C 
      • Melting Point:108-111 °C(lit.) 
      • Refractive Index:1.629 
      • Boiling Point:415.4 °C at 760 mmHg 
      • Flash Point:155.4 °C 
      • PSA:34.14000 
      • Density:1.231 g/cm3 
      • LogP:3.02440 

      2-Ethyl anthraquinone(Cas 84-51-5) Usage

      Flammability and Explosibility

      Nonflammable

      InChI:InChI=1/C16H12O2/c1-2-10-7-8-13-14(9-10)16(18)12-6-4-3-5-11(12)15(13)17/h3-9H,2H2,1H3

      84-51-5 Relevant articles

      Photocatalytically green synthesis of H2O2 using 2-ethyl-9,10-anthraquinone as an electron condenser

      Zhang, Dandan,Xu, Gangqiang,Chen, Tao,Chen, Feng

      , p. 52199 - 52202 (2014)

      A high level (~9 mM) of hydrogen peroxid...

      Hydrogen peroxide synthesis by direct photoreduction of 2-ethylanthraquinone in aerated solutions

      Ren, Ming-Guang,Mao, Mao,Duan, Xue-You,Song, Qin-Hua

      , p. 164 - 168 (2011)

      A new synthesis method of hydrogen perox...

      Engineering the porosity and acidity of H-Beta zeolite by dealumination for the production of 2-ethylanthraquinone via 2-(4′-ethylbenzoyl)benzoic acid dehydration

      Liu,He,Liu,Wang,Xin,Guo

      , p. 9731 - 9740 (2018)

      Environmentally-friendly zeolites have b...

      Role of phosphorus in the formation of selective palladium catalysts for hydrogenation of alkylanthraquinones

      Belykh, Lyudmila B.,Skripov, Nikita I.,Sterenchuk, Tatyana P.,Akimov, Vladlen V.,Tauson, Vladimir L.,Savanovich, Tatyana A.,Schmidt, Fedor K.

      , (2020)

      Effective Pd-P catalysts for the hydroge...

      Friedel - gram acylating reaction method based on phthalic anhydride and aromatic alkyl compound

      -

      Paragraph 0057-0059, (2021/09/08)

      A part of a substituted alkylbenzene is ...

      Green synthesis method for preparing 2-alkylanthraquinone from phthalic anhydride in one step

      -

      Paragraph 0036-0037; 0040-0041, (2020/06/16)

      The invention relates to the technical f...

      PROCESS FOR PRODUCING SUBSTITUTED ANTHRAQUINONE

      -

      Page/Page column 7-8; 10-11, (2020/06/10)

      A process for manufacturing a compound o...

      84-51-5 Process route

      2-(4’-ethylbenzoyl)benzoic acid
      1151-14-0

      2-(4’-ethylbenzoyl)benzoic acid

      2-ethylanthraquinone
      84-51-5

      2-ethylanthraquinone

      Conditions
      Conditions Yield
      With sulfuric acid; at 50 - 120 ℃; for 0.5h; Temperature;
      95.5%
      With fuming sulphuric acid; at 135 ℃; Temperature; Milling;
      94.3%
      2-(4’-ethylbenzoyl)benzoic acid; With thionyl chloride; at 70 ℃; for 1h;
      With aluminum (III) chloride; at 70 ℃; for 0.666667h; Temperature; Reagent/catalyst;
      94%
      With 2,6-di-tert-butyl-4-methylpyridine; at 215 ℃; for 5h; Temperature; Reagent/catalyst;
      83%
      With sulfuric acid; at 40 - 140 ℃; Temperature; Flow reactor;
      82.2%
      With phosphorus pentoxide; at 120 ℃; for 4.5h;
      76%
      Multi-step reaction with 2 steps
      1: thionyl chloride / 2 h / 50 °C
      2: trifluorormethanesulfonic acid; aluminum (III) chloride / 1,2-dichloro-ethane / 2.5 h / 55 °C
      With aluminum (III) chloride; thionyl chloride; trifluorormethanesulfonic acid; In 1,2-dichloro-ethane;
      With O40PW12(3-)*9Mg(2+)*3Al(3+)*15HO(1-)*C4H8NO3(3-); In chloroform; at 70 - 180 ℃; for 2.25h; Temperature; Reagent/catalyst;
      With perfluorosulfonic acid resin; at 130 - 200 ℃; for 1h; Temperature; Reagent/catalyst;
      With sulfuric acid; at 140 ℃; for 0.0416667h;
      2-ethyl-9,10-dihydroanthracene
      62167-65-1

      2-ethyl-9,10-dihydroanthracene

      2-ethylanthraquinone
      84-51-5

      2-ethylanthraquinone

      Conditions
      Conditions Yield
      With dinitrogen monoxide; Ru(5,10,15,20-tetramesitylporphyrin)(O)2; In benzene; at 200 ℃; under 7600 Torr;
      98%
      With dinitrogen monoxide; dioxo(tetramesitylporphyrinato)ruthenium(VI); In benzene; at 200 ℃; for 20h; under 7600 Torr;
      98%

      84-51-5 Upstream products

      • 85-44-9
        85-44-9

        phthalic anhydride

      • 100-41-4
        100-41-4

        ethylbenzene

      • 52251-71-5
        52251-71-5

        2-ethylanthracene

      • 76682-71-8
        76682-71-8

        2-ethyl-10H-9-anthranone

      84-51-5 Downstream products

      • 15547-17-8
        15547-17-8

        6-ethyl-1,2,3,4-tetrahydroanthracene-9,10-dione

      • 56600-58-9
        56600-58-9

        2-ethyl-1-nitro-9,10-anthraquinone

      • 36232-18-5
        36232-18-5

        9,10-Bis-acetylcarbamoyloxy-2-aethyl-anthracen

      • 96809-97-1
        96809-97-1

        2-Ethyl-9,10-di-(trans-styryl)-anthracen

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