6956-76-9

Usage

Uses

Used in Flavoring and Fragrance Industry:
2,2-dimethyl-2,3-dihydro-1-benzofuran-5-ol is used as a flavoring agent in the food and beverage industry for its distinctive sweet, woody aroma, enhancing the sensory experience of consumers.
Used in the Fragrance Industry:
In the fragrance industry, 2,2-dimethyl-2,3-dihydro-1-benzofuran-5-ol is utilized as an aromatic component, contributing to the creation of various scents and perfumes due to its unique olfactory characteristics.
Used in Pharmaceutical Applications:
2,2-dimethyl-2,3-dihydro-1-benzofuran-5-ol is considered for use as a therapeutic agent in pharmaceuticals, leveraging its antioxidant, anti-inflammatory, and antimicrobial properties to potentially treat various conditions. However, ongoing research is necessary to confirm its efficacy and safety in this context.
Used in Personal Care Products:
Dihydroeugenol may be used in personal care products as it possesses beneficial properties that could contribute to skin health and other personal care applications, although further investigation is required to determine its full potential and safety in these products.

Upstream product

• 38149-52-9 2-methallylhydroquinone 
• 123-31-9 hydroquinone 
• 1416157-62-4 (2,2-dimethyl-2,3-dihydrobenzofuran-5-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane 

Relevant academic research and scientific papers

SYNTHESIS AND RADICAL SCAVENGING ACTIVITY OF SUBSTITUTED DIHYDROBENZOFURAN-5-OLS

Antioxidants are important in preventing oxidative stress by scavenging oxygen free radicals. In this study, a series of 2,2-dimethyl-2,3-dihydrobenzofuran-5-ols with amino, methoxy, chloro and nitro groups at the ortho position relative tothe phenolic OH group were newly synthesized, and their galvinoxyl and hydroxyl radical scavenging activities were measured. Substituted 2,3-dihydrobenzofuran-5-ols showed higher activity than the corresponding 6-chromanols, especially 6-amino-2,2-dimethyl-2,3-dihydrobenzofuran-5-ol, which possessed the highest activity among the tested compounds. The results demonstrated that the planarity and electron-donating capacity of these molecules enhanced their radical scavenging activities, as is known for 6-chromanols.

6,7-DIHYDRO-5H-PYRROLO[3,4-B]PYRIDIN-5-ONE ALLOSTERIC MODULATORS OF THE M4 MUSCARINIC ACETYLCHOLINE RECEPTOR

The present invention is directed to 6,7-dihydro-5H-pyrrolo[3,4-b]pyridine-5-one compounds which are allosteric modulators of the M4 muscarinic acetylcholine receptor. The present invention is also directed to uses of the compounds described herein in the potential treatment or prevention of neurological and psychiatric disorders and diseases in which M4 muscarinic acetylcholine receptors are involved. The present invention is also directed to compositions comprising these compounds. The present invention is also directed to uses of these compositions in the potential prevention or treatment of such diseases in which M4 muscarinic acetylcholine receptors are involved.

Heterocyclic dioxethane substrates, process for their preparation and their use

PCT No. PCT/EP96/04506 Sec. 371 Date Apr. 20, 1998 Sec. 102(e) Date Apr. 20, 1998 PCT Filed Oct. 17, 1996 PCT Pub. No. WO97/14696 PCT Pub. Date Apr. 24, 1997Compounds of the general formula Ia and Ib are described in which R1 and R2 are the same or differ