4-Methoxystyrene
- CasNo:637-69-4
Product Description
Cost-effective and customizable 4-Methoxystyrene 637-69-4 supplier
- Molecular Formula: C9H10O
- Molecular Weight: 134.178
- Appearance/Colour: Clear colourless liquid
- Melting Point: 3.3ºC
- Refractive Index: n20/D 1.562
- Boiling Point: 220.708 °C at 760 mmHg
- Flash Point: 77.715 °C
- PSA： 9.23000
- Density: 0.963 g/cm3
- LogP: 2.33820
4-Methoxystyrene(Cas 637-69-4) Usage
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Synthesis Reference(s) |
Chemistry Letters, 13, p. 1897, 1984The Journal of Organic Chemistry, 52, p. 422, 1987 DOI: 10.1021/jo00379a020Tetrahedron Letters, 35, p. 8773, 1994 DOI: 10.1016/S0040-4039(00)78494-2 |
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General Description |
4-Methoxystyrene (also known as p-Methoxystyrene) is a chemical compound involved in photohydration reactions, where it undergoes intramolecular proton transfer. The study highlights its reactivity in comparison to other substituted styrenes, particularly noting the influence of substituents on reaction mechanisms and regioselectivity. However, the abstract does not provide specific experimental data or conclusions solely about 4-Methoxystyrene, focusing instead on broader trends among the tested compounds. Thus, no definitive conclusions about 4-Methoxystyrene itself can be drawn from this abstract. |
InChI:InChI=1/C9H10O/c1-3-8-4-6-9(10-2)7-5-8/h3-7H,1H2,2H3
637-69-4 Relevant articles
Photoredox Catalyzed Sulfonylation of Multisubstituted Allenes with Ru(bpy)3Cl2 or Rhodamine B
Chen, Jingyun,Chen, Shufang,Jiang, Jun,Lu, Qianqian,Shi, Liyang,Xu, Zekun,Yimei, Zhao
supporting information, (2021/11/09)
A highly regio- and stereoselective sulf...
Functionalized styrene synthesis via palladium-catalyzed C[sbnd]C cleavage of aryl ketones
Dai, Hui-Xiong,Wang, Xing,Wang, Zhen-Yu,Xu, Hui,Zhang, Xu
supporting information, (2022/03/31)
We report herein the synthesis of functi...
Polymerization of Allenes by Using an Iron(II) β-Diketiminate Pre-Catalyst to Generate High Mn Polymers
Durand, Derek J.,Webster, Ruth L.,Woof, Callum R.
supporting information, p. 12335 - 12340 (2021/07/19)
Herein, we report an iron(II)-catalyzed ...
Rapid synthesis method of biomass-based olefin
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Paragraph 0020; 0041-0046; 0049-0050, (2021/07/31)
The invention discloses a rapid synthesi...
637-69-4 Process route
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84648-17-9
C17 H15 ClO5
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637-69-4,24936-44-5
4-Methoxystyrene
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84648-30-6
C15 H15 ClO
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84648-24-8
3-Chloro-benzoic acid 2-(4-methoxy-phenyl)-ethyl ester
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18217-00-0
1-(2-Chloroethyl)-4-methoxybenzene
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541-73-1
1,3-Dichlorobenzene
| Conditions | Yield |
|---|---|
|
In
various solvent(s);
at 100 ℃;
Mechanism;
CIDNP, thermolyse;
|
-
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3319-15-1
rac-1-(4-methoxyphenyl)-ethanol
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-
637-69-4,24936-44-5
4-Methoxystyrene
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100-06-1
1-(4-methoxyphenyl)ethanone
| Conditions | Yield |
|---|---|
|
With
2BF4(1-)*C21H37IrN2O3(2+);
In
toluene; tert-butyl alcohol;
for 15h;
Schlenk technique;
Inert atmosphere;
Reflux;
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637-69-4 Upstream products
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917-64-6
methyl magnesium iodide
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33646-40-1
4-methoxymandelonitrile
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60-29-7
diethyl ether
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110972-63-9
4-methoxy-mandelimidic acid ethyl ester
637-69-4 Downstream products
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109562-49-4
3-(morpholin-1-yl)-1-(4-methoxyphenyl)propan-1-ol
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4648-33-3
(E)-1-methoxy-4-(4-nitrostyryl)benzene
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6142-64-9
(1R*,2R*)-ethyl 2-(4-methoxyphenyl)cyclopropanecarboxylate
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42866-92-2
2-(4-methoxyphenyl)acetaldehyde dimethyl acetal