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2-methoxy-5-(1-propenyl)phenol

  • Name 2-methoxy-5-(1-propenyl)phenol
  • CAS 501-20-2
  • Purity 99%
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Product Details

Manufacturer supply high quality 2-methoxy-5-(1-propenyl)phenol 501-20-2 with ISO standards

  • Molecular Formula: C10H12O2
  • Molecular Weight: 164.204
  • Vapor Pressure: 0.000697mmHg at 25°C 
  • Boiling Point: 298.8°Cat760mmHg 
  • Flash Point: 163.2°C 
  • PSA: 29.46000 
  • Density: 1.074g/cm3 
  • LogP: 2.43390 

2-methoxy-5-(1-propenyl)phenol(Cas 501-20-2) Usage

General Description

2-Methoxy-5-(1-propenyl)phenol (isochavibetol) is identified as a metabolite of methylisoeugenol in liver microsomes across human, rat, and bovine species, suggesting its role in the oxidative metabolic pathway. The study underscores interspecies variations in metabolite formation, with isochavibetol being one of several intermediates, alongside reactive species like 3'-oxomethylisoeugenol, which may have toxicological significance. Further research is warranted to elucidate its biological implications.

InChI:InChI=1/C10H12O2/c1-3-4-8-5-6-10(12-2)9(11)7-8/h3-7,11H,1-2H3/b4-3+

501-20-2 Relevant articles

In vivo Structure-Activity Relationship of Dihydromethysticin in Reducing Nicotine-Derived Nitrosamine Ketone (NNK)-Induced Lung DNA Damage against Lung Carcinogenesis in A/J Mice

Hati, Santanu,Hu, Qi,Huo, Zhiguang,Lu, Junxuan,Xing, Chengguo

, (2022/03/08)

Lung cancer is the leading cause of canc...

Soft template-based bismuth doped zinc oxide nanocomposites for photocatalytic depolymerization of lignin

Kausar, Samia,Ali Altaf, Ataf,Hamayun, Muhammad,Danish, Muhammad,Zubair, Muhammad,Naz, Sumbal,Muhammad, Shabbir,Zaheer, Muhammad,Ullah, Shafiq,Badshah, Amin

, (2020/01/02)

Lignin depolymerization is a growing res...

Rhodium catalyzed selective hydroaminomethylation of biorenewable eugenol under aqueous biphasic condition

Jagtap, Samadhan A.,Gowalkar, Shilpa P.,Monflier, Eric,Ponchel, Anne,Bhanage, Bhalchandra M.

, p. 108 - 116 (2018/04/17)

This work reports a highly regioselectiv...

501-20-2 Process route

piperidine
110-89-4

piperidine

chavibetol
501-19-9

chavibetol

carbon monoxide
201230-82-2

carbon monoxide

2-methoxy-4-propylphenol
58539-27-8

2-methoxy-4-propylphenol

Isochavibetol
19784-98-6,41243-66-7,501-20-2

Isochavibetol

4-(3-hydroxy-4-methoxyphenyl)butanal

4-(3-hydroxy-4-methoxyphenyl)butanal

2-methoxy-5-(4-(piperidin-1-yl)butyl)phenol

2-methoxy-5-(4-(piperidin-1-yl)butyl)phenol

C<sub>16</sub>H<sub>25</sub>NO<sub>2</sub>

C16 H25 NO2

C<sub>16</sub>H<sub>25</sub>NO<sub>2</sub>

C16 H25 NO2

Conditions
Conditions Yield
With acetylacetonato dicarbonylrhodium (I); trisodium tris(3-sulfophenyl)phosphine; hydrogen; In water; at 80 ℃; for 8h; under 22502.3 Torr; Reagent/catalyst; regioselective reaction; Inert atmosphere; High pressure;
8%Chromat.
12 %Chromat.
10 %Chromat.
With acetylacetonato dicarbonylrhodium (I); trisodium tris(3-sulfophenyl)phosphine; hydrogen; In water; at 80 ℃; for 8h; under 22502.3 Torr; Reagent/catalyst; regioselective reaction; Inert atmosphere; High pressure;
14%Chromat.
12 %Chromat.
12 %Chromat.
With acetylacetonato dicarbonylrhodium (I); trisodium tris(3-sulfophenyl)phosphine; hydrogen; In water; at 80 ℃; for 8h; under 22502.3 Torr; Temperature; Pressure; regioselective reaction; Inert atmosphere; High pressure;
9 %Chromat.
9 %Chromat.
20 %Chromat.
piperidine
110-89-4

piperidine

chavibetol
501-19-9

chavibetol

carbon monoxide
201230-82-2

carbon monoxide

2-methoxy-4-propylphenol
58539-27-8

2-methoxy-4-propylphenol

Isochavibetol
19784-98-6,41243-66-7,501-20-2

Isochavibetol

2-methoxy-5-(4-(piperidin-1-yl)butyl)phenol

2-methoxy-5-(4-(piperidin-1-yl)butyl)phenol

C<sub>16</sub>H<sub>25</sub>NO<sub>2</sub>

C16 H25 NO2

C<sub>16</sub>H<sub>25</sub>NO<sub>2</sub>

C16 H25 NO2

Conditions
Conditions Yield
With acetylacetonato dicarbonylrhodium (I); trisodium tris(3-sulfophenyl)phosphine; hydrogen; In water; at 80 ℃; for 8h; under 22502.3 Torr; regioselective reaction; Inert atmosphere; High pressure;
5 %Chromat.
6 %Chromat.

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