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2,6-Dimethoxy-1,4-benzoquinone

ALDRICH/428566 - 97%

Synonym: DMBQ

CAS Number: 530-55-2
Empirical Formula (Hill Notation): C8H8O4
Molecular Weight: 168.15
EC Number: 208-484-7
MDL Number: MFCD00016368
Linear Formula: C8H8O4
Product Type: Chemical
Catalog Number PKG Qty. Price Quantity
45-428566-5G 5 g
 $76.50
1/EA		 Add To Favorites
45-428566-25G 25 g
 $363.00
1/EA		 Add To Favorites
This picture is provided solely for illustration purposes. Optical properties of the actual product may deviate. Relevant product information is printed on labeled products and other accompanying or available information material.

This image depicts SKU: 428566-25G
This picture is provided solely for illustration purposes. Optical properties of the actual product may deviate. Relevant product information is printed on labeled products and other accompanying or available information material. This image depicts SKU: 428566-5G
This picture is provided solely for illustration purposes. Optical properties of the actual product may deviate. Relevant product information is printed on labeled products and other accompanying or available information material.

This image depicts SKU: 428566-5G

 

assay 97%
functional group ether
  ketone
InChI 1S/C8H8O4/c1-11-6-3-5(9)4-7(12-2)8(6)10/h3-4H,1-2H3
InChI key OLBNOBQOQZRLMP-UHFFFAOYSA-N
mp 253-257 °C (dec.) (lit.)
Quality Level 100 
SMILES string COC1=CC(=O)C=C(OC)C1=O
solubility DMSO: soluble(lit.)
Application: 2,6-Dimethoxy-1,4-benzoquinone may be used in the synthesis of 2-aryl-3,5-dimethoxy-1,4-benzoquinone derivatives.
Application: Known haustorial inducing factor.
General description: 2,6-Dimethoxy-1,4-benzoquinone (DBQ, 2,6-DMBQ, DMOBQ) is a 1,4-benzoquinone derivative. It is a wood allergen, has been reported to cause various skin and mucosal symptoms on exposure to wood dusts. It is formed as a product due to the activity of bacterial Azospirillum lipoferum laccase on phenolic compounds of the syringic type. DBQ is one of the components isolated from the rhizome of Gynura japonica with a potential to show anti-platelet aggregation activity in vitro. It is an anticancer agent, whose kinetics of cyclic redox transformation induced by ascorbate (AscH-) has been studied using the Clark electrode and ESR techniques. Its electrochemical reduction in acetonitrile has been studied.
Packaging: 5, 25 g in poly bottle
Purity 97%
mp 253-257 °C (dec.) (lit.)
UNSPSC 12352100

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