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Usage

Uses

Used in Pharmaceutical Applications:
1-(2,2-dimethyl-2H-chromen-6-yl)ethanol is used as a therapeutic agent for its potential in the treatment of cardiovascular and neurodegenerative disorders. Its antioxidant properties contribute to its promise in mitigating the effects of these diseases and improving overall health.
Used in the Food Industry:
In the food industry, 1-(2,2-dimethyl-2H-chromen-6-yl)ethanol is used as an additive for its antioxidant and anti-inflammatory properties. These characteristics help in preserving the quality and shelf life of various food products, ensuring consumer safety and satisfaction.
Used in Cosmetic Products:
1-(2,2-dimethyl-2H-chromen-6-yl)ethanol is also utilized as an ingredient in the cosmetic industry, where its antioxidant and anti-inflammatory properties are beneficial for skin health and the development of skincare products that promote wellness and address various skin conditions.

Upstream product

• 19013-07-1 desmethoxyencecalin 
• 99-93-4 4-Hydroxyacetophenone 
• 78-79-5 isoprene 
• 32333-31-6 2,2-dimethyl-6-acetylchroman 
• 123-08-0 4-hydroxy-benzaldehyde 
• 61370-75-0 3,4-dihydro-2,2-dimethyl-2H-1-benzopyran-6-carboxaldehyde 
• 106-44-5 p-cresol 
• 23446-57-3 2,2,6-trimethyl-3,4-dihydro-2H-chromene 
• 917-64-6 methyl magnesium iodide 
• 69964-40-5 6-formyl-2,2-dimethyl-2H-chromene 

Relevant academic research and scientific papers

FIVE DITERPENES AND OTHER CONSTITUENTS FROM NINE BACCHARIS SPECIES

Key Word Index - Baccharis spp; Compositae; diterpenes; new clerodanes; new labdanes; new flavones; new aromatics. The investigation of nine Baccharis species afforded, in addition to known compounds, three new clerodane derivatives related to bacchotricuneatin B, two ent-labdane derivatives, two 3-acetoxyflavones, a benzofuran derivative and a chromene.The overall picture of the chemistry of this large genus is still not very clear.

Synthesis of 6-(1-Hydroxyethyl)-2,2-dimethyl-2H--benzopyrans: Eupatoriachromene-C and Desmethoxyencecalinol

6-Acetyl-5,8-dimethoxy-2,2-dimethyl-2H--benzopyran (2) on reduction with potassium borohydride gives eupatoriochromene-C (1).Condensation of 4-Hydroxyacetophenone with isoprene in the presence of orthophosphoric acid gives the chroman (5) which on dehydrogenation with NBS furnishes desmethoxyencecalin (4). 4 on reduction with potassium borohydride affords desmethoxyencecalinol (3).Alternatively, 4-hydroxybenzaldehyde on condensation with isoprene gives the monochroman (6) which is also obtained by a similar condensation of 4-methylphenol with isoprene followed by reaction with DDQ.Dehydrogenation of 6 with NBS affords 6-formyl-2,2-dimethyl-2H--benzopyran (8) and 6-phenacyl bromide derivative (9). 8 on reaction with methylmagnesium iodide furnishes 3.