31005-72-8

Usage

Physical State

Colorless solid

Odor

Sweet, floral

Common Uses

Manufacturing perfumes and cosmetic products

Biological Activities

Antioxidant Properties: Potential antioxidant effects.
Anti-inflammatory Properties: May exhibit anti-inflammatory activity.

Medicinal Potential

Possible candidate for medicinal uses.

Research Needs

More research is required to fully understand its benefits and risks.

Upstream product

• 870-63-3 prenyl bromide 
• 108-46-3 recorcinol 
• 556-82-1 3-methyl-2-buten-1-ol 

Downstream Products

• 196870-74-3 7-(2'-propynyloxy)-2,2-dimethyl-3,4-dihydrobenzo[1,2-b]pyran 
• 91735-46-5 6-benzoyl-3,4-dihydro-7-hydroxy-2,2-dimethyl-2H-1-benzopyran 
• 929853-14-5 9,9-dimethyl-1,2,3,4,10,11-hexahydrobenzo[c]pyrano[3,2-g]chromen-5-one oxime 
• 96909-25-0 7-benzyloxy-6-formyl-2,2-dimethyldihydrobenzo[1,2-b]pyran 
• 97024-29-8 7-methoxy-2,2-dimethylchroman-6-carbaldehyde 
• 55215-37-7 (Z)-4-hydroxy-3-(7-hydroxy-2,2-dimethylchroman-6-yl)-5-(4-hydroxy-3-(3-methylbut-2-enyl)benzylidene)furan-2(5H)-one 
• 1422971-02-5 2-(4-hydroxyphenyl)-7,7-dimethyl-7H-furo[3,2-g]chromene 

Relevant academic research and scientific papers

Magnesium dicarboxylates promote the prenylation of phenolics that is extended to the total synthesis of icaritin

The prenylation of phenolic substrates promoted by magnesium dicarboxylates was developed. An investigation of the scope demonstrated that substrates with electron-donating group(s) gave better yields than those with electron-withdrawing group(s). Althoug

Montmorillonite clays in organic synthesis: A one-pot conversion of phenols to 2,2-dimethylbenzopyrans

2,2-Dimethylbenzopyran derivatives were generated through a one-pot Montmorillonite K10 clay-catalyzed condensation of substituted phenols with prenyl bromide.