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4-ETHYLCATECHOL

  • Product Name4-ETHYLCATECHOL
  • cas1124-39-6
  • purity99%
Inquiry

Manufacturer supply top purity 4-ETHYLCATECHOL 1124-39-6 with GMP standards

  • Molecular Formula:C8H10O2
  • Molecular Weight:138.166
  • Vapor Pressure:0.00346mmHg at 25°C 
  • Melting Point:37-40°C 
  • Refractive Index:1.578 
  • Boiling Point:273.3 °C at 760 mmHg 
  • PKA:9.90±0.10(Predicted) 
  • Flash Point:134.1 °C 
  • PSA:40.46000 
  • Density:1.159 g/cm3 
  • LogP:1.66020 

4-ETHYLCATECHOL(Cas 1124-39-6) Usage

InChI:InChI=1/C8H10O2/c1-2-6-3-4-7(9)8(10)5-6/h3-5,9-10H,2H2,1H3

1124-39-6 Relevant articles

Thermal decomposition of caffeic acid in model systems: Identification of novel tetraoxygenated phenylindan isomers and their stability in aqueous solution

Stadler, Richard H.,Welti, Dieter H.,Staempfli, Andreas A.,Fay, Laurent B.

, p. 898 - 905 (1996)

Caffeic acid subjected to mild pyrolysis...

Transetherification of guaiacol to o-ethoxyphenol with gamma Al 2O3 as a catalyst in supercritical ethanol

Yang, Le,Seshan,Li, Yongdan

, p. 36 - 39 (2013)

The production of chemicals from lignin ...

Thiols Act as Methyl Traps in the Biocatalytic Demethylation of Guaiacol Derivatives

Grimm, Christopher,Kroutil, Wolfgang,Pompei, Simona,Schiller, Christine,Schober, Lukas

, p. 16906 - 16910 (2021/07/02)

Demethylating methyl phenyl ethers is ch...

Efficient demethylation of aromatic methyl ethers with HCl in water

Bomon, Jeroen,Bal, Mathias,Achar, Tapas Kumar,Sergeyev, Sergey,Wu, Xian,Wambacq, Ben,Lemière, Filip,Sels, Bert F.,Maes, Bert U. W.

supporting information, p. 1995 - 2009 (2021/03/26)

A green, efficient and cheap demethylati...

Anchimerically Assisted Selective Cleavage of Acid-Labile Aryl Alkyl Ethers by Aluminum Triiodide and N, N-Dimethylformamide Dimethyl Acetal

Sang, Dayong,Yue, Huaxin,Zhao, Zhengdong,Yang, Pengtao,Tian, Juan

, p. 6429 - 6440 (2020/07/14)

Aluminum triiodide is harnessed by N,N-d...

Selective ether bond breaking method of aryl alkyl ether

-

Paragraph 0114-0116, (2020/09/16)

The invention discloses a selective aryl...

1124-39-6 Process route

ethyl 3-(4-(5-ethyl-2-hydroxy-3-methoxyphenoxy)-3-methoxyphenyl)propanoate

ethyl 3-(4-(5-ethyl-2-hydroxy-3-methoxyphenoxy)-3-methoxyphenyl)propanoate

4-ethylcatechol
1124-39-6

4-ethylcatechol

4-Ethylguaiacol
2785-89-9

4-Ethylguaiacol

5-ethylbenzene-1,2,3-triol
66125-16-4

5-ethylbenzene-1,2,3-triol

3-(3-methoxyphenyl)propanoic acid ethyl ester
7116-39-4

3-(3-methoxyphenyl)propanoic acid ethyl ester

ethyl 3-(4-hydroxy-3-methoxyphenyl)propanoate
61292-90-8

ethyl 3-(4-hydroxy-3-methoxyphenyl)propanoate

3-(3-hydroxy-phenyl)propionic acid ethyl ester
34708-60-6

3-(3-hydroxy-phenyl)propionic acid ethyl ester

5-ethyl-3-methoxybenzene-1,2-diol
7452-04-2

5-ethyl-3-methoxybenzene-1,2-diol

Ethyl dihydrocaffeate
3967-57-5

Ethyl dihydrocaffeate

Conditions
Conditions Yield
ethyl 3-(4-(5-ethyl-2-hydroxy-3-methoxyphenoxy)-3-methoxyphenyl)propanoate; With platinum-nickel nanoclusters on activated carbon; hydrogen; potassium hexamethylsilazane; In m-xylene; at 180 ℃; for 18h; under 775.743 Torr;
With N,O-Bis(trimethylsilyl)trifluoroacetamide; In m-xylene; at 65 ℃; for 1h; Overall yield = 41 %;
15 %Chromat.
20 %Chromat.
13 %Chromat.
7 %Chromat.
4 %Chromat.
4 %Chromat.
2 %Chromat.
< 2 %Chromat.
5-ethyl-2-methoxyphenol
2785-88-8

5-ethyl-2-methoxyphenol

4-ethylcatechol
1124-39-6

4-ethylcatechol

4-Ethylguaiacol
2785-89-9

4-Ethylguaiacol

Conditions
Conditions Yield
With 3-mercaptopropionic acid ethyl ester; In aq. buffer; at 30 ℃; for 24h; pH=6.5; Inert atmosphere; Glovebox; Enzymatic reaction;

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    4-(benzo[d]oxazol-2'-ylthio)-5-ethylbenzene-1,2-diol

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    4-(benzo[d]thiazol-2'-ylthio)-5-ethylbenzene-1,2-diol

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