97399-70-7

Basic information

• Product Name: 8,9-Dihydro-1-methylphenanthro[1,2-b]furan-6,10,11(7H)-trione
• Synonyms: 8,9-Dihydro-1-methylphenanthro[1,2-b]furan-6,10,11(7H)-trione;Nortanshinone
• CAS NO: 97399-70-7
• Molecular Formula: C₁₇H₁₂O₄
• Molecular Weight: 280.27
• Mol File: 97399-70-7.mol
• Article Data: 2

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 8,9-Dihydro-1-methylphenanthro[1,2-b]furan-6,10,11(7H)-trione(CAS DataBase Reference)
• NIST Chemistry Reference: 8,9-Dihydro-1-methylphenanthro[1,2-b]furan-6,10,11(7H)-trione(97399-70-7)
• EPA Substance Registry System: 8,9-Dihydro-1-methylphenanthro[1,2-b]furan-6,10,11(7H)-trione(97399-70-7)

Safety Data

• Hazardous Substances Data: 97399-70-7(Hazardous Substances Data)

Usage

Description

8,9-Dihydro-1-methylphenanthro[1,2-b]furan-6,10,11(7H)-trione is a complex organic compound with a unique molecular structure that features a phenanthrene fused with a furan ring. 8,9-Dihydro-1-methylphenanthro[1,2-b]furan-6,10,11(7H)-trione is characterized by its tricyclic system and multiple functional groups, which contribute to its potential applications in various fields.

Uses

Used in Pharmaceutical Industry:
8,9-Dihydro-1-methylphenanthro[1,2-b]furan-6,10,11(7H)-trione is used as a therapeutic agent for treating bacterial infections. Its chemical structure allows it to target and inhibit the growth of harmful bacteria, providing an effective treatment option for various infections.
Used in Anti-Inflammatory Applications:
In the field of anti-inflammatory agents, 8,9-Dihydro-1-methylphenanthro[1,2-b]furan-6,10,11(7H)-trione is utilized for its ability to reduce inflammation and protect bones. Its anti-inflammatory properties can help alleviate pain and swelling associated with various conditions, while also promoting bone health and preventing bone loss.
Used in Cosmetic Industry:
8,9-Dihydro-1-methylphenanthro[1,2-b]furan-6,10,11(7H)-trione can also be found in cosmetic products due to its potential benefits for skin health. Its unique molecular structure may contribute to improved skin hydration, elasticity, and overall appearance, making it a valuable ingredient in skincare formulations.
Used in Research and Development:
Due to its complex structure and potential applications, 8,9-Dihydro-1-methylphenanthro[1,2-b]furan-6,10,11(7H)-trione is also used in research and development settings. Scientists and researchers explore its properties and potential uses in various industries, including pharmaceuticals, cosmetics, and materials science, to further understand its capabilities and develop new applications.

Upstream product

• 118949-96-5 2-vinylcyclohex-2-en-1-one ethylene glycol ketal 
• 113297-21-5 4,5-dihydro-3-methylbenzo[1,2-b]furan-4,5-dione 
• 78881-14-8 2-Hydroxy-1-cyclohexanon-ethylenacetal 
• 7182-21-0 5-hydroxy-3-methylbenzo<1.2-b>furan 
• 4746-96-7 1,4-dioxaspiro[4.5]decan-6-one 
• 70156-98-8 6-bromo-1,4-dioxaspiro[4,5]dec-6-ene 
• 127665-65-0 2-iodo-2-cyclohexen-1-one ethylene glycol ketal 
• 127665-66-1 2-hydroxy-2-cyclohexen-1-one 2-triflate ethylene glycol ketal 

Relevant articles and documents

Ultrasound-Promoted Cycloadditions in the Synthesis of Salvia miltiorrhiza Abietanoid o-Quinones

The ultrasound-promoted Diels-Alder reaction of 3-methyl-4,5-benzofurandione with appropriately substituted vinylcyclohexenes has led to the synthesis of tanshinone IIA, nortanshinone, tanshindiol B, methyl tanshinonate, and tanshinone IIB, biologically active metabolites of the Chinese traditional medicine, Dan Shen, prepared from the roots of Salvia miltiorrhiza Bunge.Methyltanshinquinone, the dihydro derivative of the natural product, methylenetanshinquinone, was similarly prepared.The effect of ultrasound in promoting the cycloadditions parallels that of high pressure and improved the regioselectivity in favour of the natural isomers.