CAS 36379-74-5

7,9-Dimethoxy-3-methyl-1H-naphtho[2,3-c]pyran-5,10-dione

Description:

7,9-Dimethoxy-3-methyl-1H-naphtho[2,3-c]pyran-5,10-dione, with the CAS number 36379-74-5, is a synthetic organic compound characterized by its complex polycyclic structure, which includes a naphthoquinone moiety. This compound features two methoxy groups at the 7 and 9 positions and a methyl group at the 3 position of the naphthalene ring, contributing to its unique chemical properties. It is known for its potential biological activities, including antioxidant and antimicrobial properties, which have garnered interest in medicinal chemistry and pharmacology. The presence of the dione functional groups indicates that it can participate in various chemical reactions, such as nucleophilic additions or redox reactions. Its solubility may vary depending on the solvent, and it is typically analyzed using techniques like NMR spectroscopy and mass spectrometry for structural elucidation. Overall, 7,9-Dimethoxy-3-methyl-1H-naphtho[2,3-c]pyran-5,10-dione represents a fascinating compound within the realm of organic chemistry, with potential applications in drug development and other fields.

Formula: C₁₆H₁₄O₅

InChI: InChI=1S/C16H14O5/c1-8-4-10-12(7-21-8)16(18)14-11(15(10)17)5-9(19-2)6-13(14)20-3/h4-6H,7H2,1-3H3

InChI key: InChIKey=ITUSOEBAIVROCD-UHFFFAOYSA-N

SMILES: O=C1C=2C(C(=O)C3=C1COC(C)=C3)=CC(OC)=CC2OC

Synonyms:

• 7,9-Dimethoxy-3-methyl-1H-naphtho[2,3-c]pyran-5,10-dione
• 3,4-Didehydro-3-deoxyherbarin
• Anhydroherbarin
• 1H-Naphtho[2,3-c]pyran-5,10-dione, 7,9-dimethoxy-3-methyl-
• Dehydroherbarin

Dehydroherbarin

CAS: 36379-74-5

Dehydroherbarin is a natural product for research related to life sciences. The catalog number is TN5794 and the CAS number is 36379-74-5.

Formula: C₁₆H₁₄O₅

Purity: 98%

Color and Shape: Solid

Molecular weight: 286.28

Ref: TM-TN5794

Dehydroherbarin

CAS: 36379-74-5

**Dehydroherbarin** is a naturally occurring naphthoquinone, which is a secondary metabolite derived from certain fungi species. This compound is synthesized within the fungal metabolism and serves a variety of ecological functions, including defense mechanisms against microorganisms. Dehydroherbarin operates through oxidative and reductive pathways, displaying potent activity in redox reactions. This mode of action is attributed to its ability to interact with cellular components, effectively modulating oxidative stress within biological systems.

Formula: C₁₆H₁₄O₅

Purity: Min. 95%

Molecular weight: 286.28 g/mol

Ref: 3D-LBA37974