98154-04-2

Basic information

• Product Name: 7-HYDROXY-4-METHOXY-INDAN-1-ONE
• Synonyms: 7-HYDROXY-4-METHOXY-1-INDANONE;7-HYDROXY-4-METHOXY-INDAN-1-ONE;7-Hydroxy-4-methoxy-2,3-dihydroinden-1-one
• CAS NO: 98154-04-2
• Molecular Formula: C₁₀H₁₀O₃
• Molecular Weight: 178.186
• Mol File: 98154-04-2.mol

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 7-HYDROXY-4-METHOXY-INDAN-1-ONE(CAS DataBase Reference)
• NIST Chemistry Reference: 7-HYDROXY-4-METHOXY-INDAN-1-ONE(98154-04-2)
• EPA Substance Registry System: 7-HYDROXY-4-METHOXY-INDAN-1-ONE(98154-04-2)

Safety Data

• Hazardous Substances Data: 98154-04-2(Hazardous Substances Data)

Usage

Uses

Used in Fragrance and Flavor Industry:
7-HYDROXY-4-METHOXY-INDAN-1-ONE is used as a fragrance and flavor ingredient for its pleasant and sweet aroma. It is commonly used in perfumes, soaps, and other personal care products to enhance their scent and appeal to consumers.
Used in Beauty Industry:
In the beauty industry, 7-HYDROXY-4-METHOXY-INDAN-1-ONE is used as an ingredient in various cosmetic products, such as creams, lotions, and serums, due to its potential anti-inflammatory and antioxidant properties. These properties may contribute to skin health and protection against environmental stressors.
Used in Healthcare Industry:
7-HYDROXY-4-METHOXY-INDAN-1-ONE has been studied for its potential therapeutic properties in the healthcare industry. Its anti-inflammatory effects may be beneficial in managing conditions such as arthritis and other inflammatory disorders. Additionally, its antioxidant properties may help protect cells from damage caused by free radicals, potentially reducing the risk of chronic diseases.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 7-HYDROXY-4-METHOXY-INDAN-1-ONE is being researched for its potential use in developing new drugs and treatments. Its anti-inflammatory and antioxidant properties may be harnessed to create medications for various health conditions, including inflammatory diseases and oxidative stress-related disorders.

Upstream product

• 52428-09-8 4,7-dimethoxyindan-1-one 
• 10538-51-9 2,5-dimethoxycinnamic acid 
• 10538-49-5 3-(2,5-dimethoxyphenyl)propanoic acid 
• 100126-94-1 3-(2,5-dimethoxyphenyl)propionyl chloride 

Relevant articles and documents

Furan Derivatives. Part 6. On Effect of Ring Size in Synthesis of 4,5-Dihydro-3H-naphthofurans and Their Analogues

Furan derivatives have been synthesized from 7-hydroxy-4-methoxy-2,3-dihydroinden-1-one (7b), 8-hydroxy-5-methoxy-1,2,3,4-tetrahydronaphthalen-1-one (4b), 4-hydroxy-1-methoxy-6,7,8,9-tetrahydro-5H-benzocyclohepten-5-one (8b), 6-hydroxy-2a,3-dihydro-2H-naphthofuran-5(4H)-one (9b), 7-hydroxy-2,3,3a,4-tetrahydronaphthopyran-6(5H)-one (10b), and 7-hydroxy-2,2a,3,4-tetrahydrocycloheptabenzofuran-6(5H)-one (11b).Hydroxy ketones such as (4b), (8b), (10b), and (11b) which have a strong intramolecular hydrogen bond between the hydroxy and the carbonyl groups easily produced the furan derivatives (1), (13), (15), and (16).However, the hydroxy ketones (7b) and (9b) in which the intramolecular hydrogen bond was weak failed to give the furan derivatives (12) and (14).