What is the 3,4-DIMETHOXYSTYRENE?

3,4-DIMETHOXYSTYRENE is , while it's Molecular Formula is C10H12O2. 3,4-Dimethoxy Styrene (~1% Hydroquinone as stabilizer) (cas# 6380-23-0) is a compound useful in organic synthesis.

What is the CAS number for 3,4-DIMETHOXYSTYRENE?

The CAS number of 3,4-DIMETHOXYSTYRENE is 6380-23-0.

What is the 3,4-DIMETHOXYSTYRENE?

3,4-DIMETHOXYSTYRENE is , while it's Molecular Formula is C10H12O2. 3,4-Dimethoxy Styrene (~1% Hydroquinone as stabilizer) (cas# 6380-23-0) is a compound useful in organic synthesis.

What is the CAS number for 3,4-DIMETHOXYSTYRENE?

The CAS number of 3,4-DIMETHOXYSTYRENE is 6380-23-0.

3,4-DIMETHOXYSTYRENE

Factory Sells Best Quality 3,4-DIMETHOXYSTYRENE 6380-23-0 with GMP standards

Molecular Formula:C10H12O2
Molecular Weight:164.204
Vapor Pressure:0.021mmHg at 25°C
Refractive Index:n20/D 1.571(lit.)
Boiling Point:259.4 °C at 760 mmHg
Flash Point:95.9 °C
PSA：18.46000
Density:1.004 g/cm³
LogP:2.34680

3,4-DIMETHOXYSTYRENE(Cas 6380-23-0) Usage

Synthesis Reference(s)

Tetrahedron Letters, 21, p. 3451, 1980 DOI: 10.1016/S0040-4039(00)78712-0

InChI:InChI=1/C10H12O2/c1-4-8-5-6-9(11-2)10(7-8)12-3/h4-7H,1H2,2-3H3

6380-23-0 Relevant articles

Cathodic Regioselective Coupling of Unactivated Aliphatic Ketones with Alkenes

Wu, Hongting,Chen, Weihao,Deng, Weijie,Yang, Ling,Li, Xinling,Hu, Yunfei,Li, Yibiao,Chen, Lu,Huang, Yubing

supporting information, p. 1412 - 1417 (2022/02/23)

A regioselective coupling of aliphatic k...

Olefination via Cu-Mediated Dehydroacylation of Unstrained Ketones

Dong, Guangbin,Xu, Yan,Zhou, Xukai

supporting information, p. 20042 - 20048 (2021/12/03)

The dehydroacylation of ketones to olefi...

Nickel-Catalyzed Enantioselective Hydroboration of Vinylarenes

Stanley, Levi M.,Tran, Hai N.

supporting information, (2021/12/27)

The enantioselective hydroboration of vi...

Efficient synthesis of styrene derivatives through ethenolysis of renewable propenylbenzenes

Avenda?o Villarreal, Jesus A.,Delolo, Fábio G.,Granato, Artur V.,dos Santos, Eduardo N.

, (2021/06/03)

Functionalized styrenes were obtained by...

6380-23-0 Process route

: 67-71-0
dimethylsulfone

: 93-03-8
(3,4-dimethoxyphenyl)methanol

: 6380-23-0
3,4-dimethoxystyrene

: 1333-74-0
hydrogen

Conditions

Conditions	Yield
With 1,10-Phenanthroline; potassium tert-butylate; iron(II) chloride; In toluene; at 120 ℃; for 24h; Inert atmosphere; Schlenk technique;	74%

lignin, softwood Kraft black liquor: lignin, softwood Kraft black liquor

: 95-87-4
2,5-Dimethylphenol

: 6380-23-0
3,4-dimethoxystyrene

: 106-44-5
p-cresol

: 620-17-7
3-ethylphenol

: 93-51-6
2-Methoxy-4-methylphenol

: 2785-87-7
2-methoxy-4-n-propylphenol

: 4463-33-6
1,2-dimethoxy-3-methylbenzene

: 3209-13-0
O-methylorcinol

: 2896-67-5
2-methyl-6-methoxyphenol

: 7786-61-0,31853-85-7
3-methoxy-4-hydroxystyrene

: 2785-89-9
4-Ethylguaiacol

: 24599-58-4
2,5-dimethoxy toluene

: 5932-68-3
(E)-2-methoxy-4-(1-propenyl)phenol

: 2503-46-0
1-(4-hydroxy-3-methoxyphenyl)2-propanone

: 14059-92-8
4-ethylsyringol

: 121-33-5,8014-42-4
vanillin

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

: 90-05-1
2-methoxy-phenol

: 498-02-2
1-(3-methoxy-4-hydroxyphenyl)ethanone

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

Conditions

Conditions	Yield
at 650 ℃; for 0.00555556h; Pyrolysis;

6380-23-0 Upstream products

110-86-1
pyridine
50919-04-5
4-(1-chloro-ethyl)-1,2-dimethoxy-benzene
917-64-6
methyl magnesium iodide
120-14-9
3,4-dimethoxy-benzaldehyde

6380-23-0 Downstream products

69151-24-2
4-(1,2-dibromo-ethyl)-1,2-dimethoxy-benzene
86980-84-9
2-(3,4-Dimethoxyphenyl)-2,3,3a,4,5,6-hexahydropyrrolo<1,2-b>isoxazole
79235-48-6
2-(3,4-Dimethoxy-phenyl)-hexahydro-isoxazolo[2,3-a]pyridine
112840-47-8
1-chloro-1-methyl-2-(3,4-dimethoxyphenyl)cyclopropane