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Factory Sells Best Quality O-TOLYL ACETATE 533-18-6 with ISO standards

  • Molecular Formula: C9H10O2
  • Molecular Weight: 150.177
  • Refractive Index: 1.4980-1.5010 
  • Boiling Point: 207.2 °C at 760 mmHg 
  • Flash Point: 84 °C 
  • PSA: 26.30000 
  • Density: 1.047 g/cm3 
  • LogP: 1.92030 

O-TOLYL ACETATE(Cas 533-18-6) Usage

Preparation

From sodium o-cresol and acetic anhydride.

InChI:InChI=1/C9H10O2/c1-7-5-3-4-6-9(7)11-8(2)10/h3-6H,1-2H3

533-18-6 Relevant articles

Submicron ZnO raspberries as effective catalysts for Fries rearrangement

Ali, Mohammed,Rahaman, Hasimur,Pal, Sudip Kumar,Kar, Nikita,Ghosh, Sujit Kumar

, p. 41780 - 41785 (2015)

o-Xylene-in-water emulsion droplets have...

Method for promoting acylation of amine or alcohol by carbon dioxide

-

Paragraph 0034-0035, (2021/05/29)

The invention relates to a method for pr...

An efficient method to prepare aryl acetates by the carbonylation of aryl methyl ethers or phenols

Zhang, Dejin,Yang, Guoqiang,Xiong, Junping,Liu, Jia,Hu, Xingbang,Zhang, Zhibing

, p. 2683 - 2687 (2021/02/16)

Synthesis of valuable chemicals from lig...

Steric effect of NHC ligands in Pd(II)–NHC-catalyzed non-directed C–H acetoxylation of simple arenes

Mandal, Tanmoy,Yadav, Sudha,Choudhury, Joyanta

, (2021/09/06)

Although there has been a lot of progres...

Synthetic method of benzofuranone

-

Paragraph 0066-0070, (2020/06/16)

The invention provides a synthetic metho...

533-18-6 Process route

potassium thioacetate
10387-40-3

potassium thioacetate

phenol
108-95-2,27073-41-2

phenol

2-methylphenyl acetate
533-18-6

2-methylphenyl acetate

Conditions
Conditions Yield
With carbon dioxide; at 100 ℃; for 14h; under 760.051 Torr;
83%
acetic anhydride
108-24-7

acetic anhydride

ortho-cresol
95-48-7,77504-84-8

ortho-cresol

2-methylphenyl acetate
533-18-6

2-methylphenyl acetate

Conditions
Conditions Yield
at 20 ℃; for 0.666667h;
100%
With triethylamine; In dichloromethane; at 20 ℃;
99%
With silver trifluoromethanesulfonate; at 60 ℃; for 0.116667h; neat (no solvent);
99%
With magnesium; In neat (no solvent); at 25 ℃; for 18h; Temperature;
98%
With lithium bis(perfluorooctylsulfonyl)amide; at 40 ℃; for 48h; Reagent/catalyst; Temperature; Catalytic behavior;
97%
In toluene; for 2h; Reflux;
96%
With N-methylmorpholinium propanesulfonic acid ammonium hydrogensulfate; at 25 ℃; for 0.05h; chemoselective reaction; Inert atmosphere; neat (no solvent);
95%
With zirconium phosphate; In neat (no solvent); at 60 ℃; for 1h; Green chemistry;
95%
With (2,3,4,5,6-pentafluorophenyl)ammonium triflate; In neat (no solvent); at 20 ℃; for 0.666667h;
95%
Sulfate; tin(IV) oxide; at 20 ℃; for 0.333333h;
94%
With nickel zirconium phosphate; In neat (no solvent); at 40 ℃; for 0.25h;
93%
sulfuric acid; for 1h; Heating;
92%
With Cu(2+)*Zr(4+)*2PO4(3-) = CuZr(PO4)2; at 60 ℃; for 0.5h;
92%
With iron zirconium phosphate; In neat (no solvent); at 40 ℃; for 0.25h; Green chemistry;
91%
Montmorillonite KSF; for 3.5h; Ambient temperature;
90%
With Montmorillonite KSF; for 3.5h; Ambient temperature;
90%
With phosphorus pentoxide; silica gel; at 20 ℃; for 0.333333h;
90%
With multi-walled carbonnanotubes functionalized with phosphonic acid; In neat (no solvent); at 20 ℃; for 1.33333h;
85%
With sodium hydroxide;
75%
With sulfuric acid;
With sodium hydroxide;
With sodium acetate;
With pyridine;
chloromethyl polystyrene supported gadolinium triflate; In dimethyl sulfoxide; at 20 ℃; for 0.5h;
99 % Chromat.
With sulfuric acid;
With 1-butyl-3-methylimidazolium 4-methylbenzenenesulfonate; 1-butyl-3-methylimidazolium Tetrafluoroborate; at 50 ℃; for 0.666667h;
95 %Chromat.
With iron(III) phosphate; at 20 ℃; for 11h; chemoselective reaction;
92 %Chromat.
With 5,10,15,20-tetraphenylporphyrinatovanadium(IV) trifluoromethanesulfonate; In acetonitrile; at 20 ℃; for 0.0333333h;
98 %Chromat.
With C13H16NO6S2(1+)*HO4S(1-); at 25 ℃; for 0.116667h; Green chemistry;
97 %Chromat.
With triethylamine; In dichloromethane; at 20 ℃; for 12h;
With pyridine; at 100 ℃;
With potassium carbonate; In dichloromethane; at 20 ℃; for 24h;
at 150 ℃; for 3h;
With sulfuric acid; at 20 ℃; for 0.5h;

533-18-6 Upstream products

  • 127-09-3
    127-09-3

    sodium acetate

  • 108-24-7
    108-24-7

    acetic anhydride

  • 95-48-7
    95-48-7

    ortho-cresol

  • 64-19-7
    64-19-7

    acetic acid

533-18-6 Downstream products

  • 704-65-4
    704-65-4

    2-(bromomethyl)phenyl acetate

  • 876-02-8
    876-02-8

    4-hydroxy-3-methylphenyl methyl ketone

  • 699-91-2
    699-91-2

    2-acetyl-6-methylphenol

  • 855354-81-3
    855354-81-3

    acetic acid-(4-iodo-2-methyl-phenyl ester)

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