1,4-Dimethoxybenzene

Synonym: NSC 7483; p-Methoxyanisole; Dimethylhydroquinone; Hydroquinone dimethyl ether
Molecular Formula: C6H4(OCH3)2; C8H10O2
Molecular Weight: 138.16
CAS Number: 150-78-7
MDL number: MFCD00008401
EC Number: 205-771-9
Note: Prices are for comparison only. Contact Sales for current pricing.
Purity: 99 %
Packing size: 100 MG  
Form: crystals  
46.55 EUR
Purity: 99 %
Packing size: 1 KG  
Form: crystals  
59.64 EUR
Purity: 99 %
Packing size: 5 KG  
Form: crystals  
205.10 EUR
Purity: 99 %
Packing size: 10 KG  
Form: crystals  
317.10 EUR
Purity: 99 %
Packing size: 500 G  
Form: crystals  
48.37 EUR
Purity: 99 %
Packing size: 1 KG  
Form: crystals  
95.90 EUR
Purity: 99 %
Packing size: 100 G  
Form: crystals  
19.60 EUR

 Product Description

1,4-DIMETHOXYBENZENE is a chemical compound featuring two methoxy groups attached to a benzene ring. It is commonly used as a building block in organic synthesis for the preparation of various aromatic compounds.

 

Application:

1,4-DIMETHOXYBENZENE serves as a key intermediate in the synthesis of pharmaceuticals, agrochemicals, and fragrances. It is utilized in the production of dyes, antioxidants, and specialty chemicals as well.

 

 

 

Articles:

- 2-Chloro-1,4-Dimethoxybenzene as a Novel Catalytic Cofactor for Oxidation of Anisyl Alcohol by Lignin Peroxidase

Publication Date: 1 March 1998

Pauline J. M. Teunissen, Jim A. Field

https://doi.org/10.1128/AEM.64.3.830-835.1998

 

- 2-Chloro-1,4-dimethoxybenzene as a mediator of lignin peroxidase catalyzed oxidations

Publication Date: Available online 3 December 1998

Pauline J.M Teunissen, Jim A Field

https://doi.org/10.1016/S0014-5793(98)01386-6

 

- Combining 1,4-dimethoxybenzene, the major flower volatile of wild strawberry Fragaria vesca, with the aggregation pheromone of the strawberry blossom weevil Anthonomus rubi improves attraction

Publication Date: Available online 7 July 2014

Atle Wibe, Anna-Karin Borg-Karlson, Jerry Cross, Helena Bichão, Michelle Fountain, Ilme Liblikas, Lene Sigsgaard

https://doi.org/10.1016/j.cropro.2014.06.016