2-methoxy-5-(1-propenyl)phenol
- Name 2-methoxy-5-(1-propenyl)phenol
- CAS 501-20-2
- Purity 99%
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
-
-
110-89-4
piperidine
-
-
501-19-9
chavibetol
-
-
201230-82-2
carbon monoxide
-
-
58539-27-8
2-methoxy-4-propylphenol
-
-
19784-98-6,41243-66-7,501-20-2
Isochavibetol
-
-
4-(3-hydroxy-4-methoxyphenyl)butanal
-
-
2-methoxy-5-(4-(piperidin-1-yl)butyl)phenol
-
-
C16 H25 NO2
-
-
C16 H25 NO2
| 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. |
-
-
110-89-4
piperidine
-
-
501-19-9
chavibetol
-
-
201230-82-2
carbon monoxide
-
-
58539-27-8
2-methoxy-4-propylphenol
-
-
19784-98-6,41243-66-7,501-20-2
Isochavibetol
-
-
2-methoxy-5-(4-(piperidin-1-yl)butyl)phenol
-
-
C16 H25 NO2
-
-
C16 H25 NO2
| 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. |
501-20-2 Upstream products
-
621-59-0
isovanillin
-
10467-10-4
ethylmagnesium iodide
-
64-17-5
ethanol
-
145134-27-6
1-methoxy-2-methoxymethoxy-4-trans -propenyl-benzene
501-20-2 Downstream products
-
1258741-40-0
5-(1-(2,4-dimethoxyphenyl)propyl)-2-methoxyphenol
-
38146-61-1
6-(3-hydroxy-4-methoxyphenethyl)-4-methoxy-5,6-dihydro-2H-pyran-2-one
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