CAS 21086-65-7

4,5-Dimethoxy-1,2-benzoquinone

Description:

4,5-Dimethoxy-1,2-benzoquinone is an organic compound characterized by its quinone structure, which features a six-membered aromatic ring with two methoxy groups (-OCH3) attached to the 4 and 5 positions. This compound is typically a yellow to orange solid at room temperature and is known for its reactivity due to the presence of the quinone functional group, which can participate in various chemical reactions, including oxidation and reduction processes. It is soluble in organic solvents such as ethanol and acetone but has limited solubility in water. The methoxy groups enhance its electron-donating properties, influencing its reactivity and stability. 4,5-Dimethoxy-1,2-benzoquinone is of interest in organic synthesis and may have applications in the development of dyes, pigments, or as an intermediate in the synthesis of other chemical compounds. Safety precautions should be taken when handling this substance, as quinones can be toxic and may cause skin or respiratory irritation.

Formula: C₈H₈O₄

InChI: InChI=1S/C8H8O4/c1-11-7-3-5(9)6(10)4-8(7)12-2/h3-4H,1-2H3

InChI key: InChIKey=DCNHYWSNHGOKHN-UHFFFAOYSA-N

SMILES: O(C)C=1C(OC)=CC(=O)C(=O)C1

Synonyms:

• 3,5-Cyclohexadiene-1,2-dione, 4,5-dimethoxy-
• 4,5-Dimethoxy-1,2-benzoquinone
• 4,5-Dimethoxy-3,5-cyclohexadiene-1,2-dione
• 4,5-Dimethoxycyclohexa-3,5-Diene-1,2-Dione
• NSC 121600
• o-Benzoquinone, 4,5-dimethoxy-
• 4,5-Dimethoxy-o-benzoquinone

3,5-Cyclohexadiene-1,2-dione, 4,5-dimethoxy-

CAS: 21086-65-7

Formula: C₈H₈O₄

Molecular weight: 168.1467

Ref: IN-DA002L0U

4,5-Dimethoxy-1,2-benzoquinone

CAS: 21086-65-7

4,5-Dimethoxy-1,2-benzoquinone is an organic compound, which is derived from various plant sources, particularly certain fungi and lichen species. This compound is characterized by its benzoquinone structure with two methoxy groups, contributing to its reactive nature. It functions primarily through redox cycling, engaging in electron transfer processes that can influence cellular oxidative states. This mode of action allows it to either promote or inhibit oxidative stress, depending on the specific biochemical context.

Formula: C₈H₈O₄

Purity: Min. 95%

Color and Shape: Powder

Molecular weight: 168.15 g/mol

Ref: 3D-FD66679