CAS 19643-45-9
:2,6-Dibromo-1,4-benzoquinone
Description:
2,6-Dibromo-1,4-benzoquinone is an organic compound characterized by its structure, which features a quinone moiety with two bromine substituents at the 2 and 6 positions of the benzene ring. This compound is typically a yellow to orange solid, exhibiting a strong aromatic character due to the presence of the conjugated double bonds in the quinone structure. It is known for its reactivity, particularly in electrophilic substitution reactions, owing to the electron-withdrawing nature of the quinone and bromine groups. The compound is soluble in organic solvents, such as dichloromethane and acetone, but has limited solubility in water. 2,6-Dibromo-1,4-benzoquinone is utilized in various chemical applications, including as a reagent in organic synthesis and as a potential intermediate in the production of dyes and pharmaceuticals. Additionally, it may exhibit biological activity, making it of interest in medicinal chemistry. As with many brominated compounds, it is important to handle it with care due to potential toxicity and environmental concerns.
Formula:C6H2Br2O2
InChI:InChI=1S/C6H2Br2O2/c7-4-1-3(9)2-5(8)6(4)10/h1-2H
InChI key:InChIKey=FGHCYIPZQUMLRQ-UHFFFAOYSA-N
SMILES:O=C1C(Br)=CC(=O)C=C1Br
Synonyms:- 2,5-Cyclohexadiene-1,4-dione, 2,6-dibromo-
- 2,6-Dibromo-1,4-benzoquinone
- 2,6-Dibromo-2,5-cyclohexadiene-1,4-dione
- 2,6-Dibromobenzoquinone
- 2,6-Dibromocyclohexa-2,5-Diene-1,4-Dione
- 2,6-Dibromoquinone
- Nsc 294731
- p-Benzoquinone, 2,6-dibromo-
- 2,6-Dibromo-p-benzoquinone
- 2,6-Dibromo-p-benzoquinone
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Found 5 products.
2,6-Dibromo-p-benzoquinone
CAS:Formula:C6H2Br2O2Purity:98%Color and Shape:SolidMolecular weight:265.88692,6-Dibromocyclohexa-2,5-diene-1,4-dione
CAS:2,6-Dibromocyclohexa-2,5-diene-1,4-dionePurity:98%Molecular weight:265.89g/mol2,6-Dibromoquinone
CAS:Controlled ProductFormula:C6H2Br2O2Color and Shape:Yellow CrystallineMolecular weight:265.892,6-Dibromo-1,4-benzoquinone
CAS:<p>2,6-Dibromo-1,4-benzoquinone is an organic compound that has been shown to be genotoxic in the bladder. It reacts with hydrochloric acid to form a dibrominated diphenyl ether, which can undergo a number of reactions. 2,6-Dibromo-1,4-benzoquinone produces reactive hydroxyl groups and chemical structures that are carcinogenic. The reaction mechanism is not well understood but it has been shown to inhibit DNA synthesis and cause cancer in laboratory animals. 2,6-Dibromo-1,4-benzoquinone also inhibits RNA synthesis and protein synthesis by forming covalent bonds with amino acids in the ribosome or by reacting with nucleotides in DNA molecules. This leads to cell death as cells are unable to synthesize proteins for growth and repair.</p>Formula:C6H2Br2O2Purity:Min. 95%Color and Shape:PowderMolecular weight:265.89 g/mol




