30574-34-6

Usage

Physical state

Colorless liquid

Odor

Sweet, floral

Uses

Production of fragrances and flavorings; perfumes and cosmetics; intermediate in the synthesis of pharmaceuticals and other organic compounds

Properties

Antimicrobial and antifungal activities

Potential applications

Development of new antimicrobial agents.

Upstream product

• 613-84-3 2-hydroxy-5-methylbenzaldehyde 
• 7083-19-4 2-methoxy-5-methylbenzaldehyde 
• 104-93-8 p-methylanizole 
• 79-30-1 isobutyryl chloride 
• 64207-03-0 1-(2-hydroxy-5-methylphenyl)-2-methylpropan-1-one 
• 77-78-1 dimethyl sulfate 

Downstream Products

• 30543-91-0 litseachromolaevane A 
• 130633-10-2 5-hydroxy-5-(2'-methoxy-5'-methylphenyl)-6-methylheptan-2-one 
• 74285-00-0 4-(2-methyloxy-5-methylphenyl)-5-methylhexanoic acid 
• 30646-07-2 3-(2-methyloxy-5-methylphenyl)-4-methylpentan-1-ol 
• 30543-93-2 ethyl 3-(2-methyloxy-5-methylphenyl)-4-methylpentanoate 
• 73256-96-9 6-Methyl-5-(2'-methoxy-5'-methylphenyl)-3-hepten-2-on 
• 73256-95-8 3-Methyl-2-(2'-methoxy-5'-methylphenyl)-1-butanal 
• 815620-60-1 tert-butyl-[5-(2-methoxy-5-methyl-phenyl)-4,4-dimethyl-hex-5-enyloxy]-dimethyl-silane 
• 815620-59-8 5-(tert-butyl-dimethyl-silanyloxy)-1-(2-methoxy-5-methyl-phenyl)-2,2-dimethyl-pentan-1-one 
• 815620-61-2 5-(2-methoxy-5-methyl-phenyl)-4,4-dimethyl-hex-5-en-1-ol 
• 815620-64-5 [1-(2'-methoxy-5'-methylphenyl)-2,2-dimethylcyclopentyl]-methanol 
• 815620-58-7 5-hydroxy-1-(2-methoxy-5-methyl-phenyl)-2,2-dimethyl-pentan-1-one 

Relevant academic research and scientific papers

Novel anti-neurodegenerative natural compounds isolated from Alpiniae Oxyphyllae Fructus and their total synthesis

This invention is directed to novel compounds isolated or derived from Alpiniae oxyphyllae fructus, chemically synthesized novel compounds, methods of preparing the novel compounds and uses thereof as neuroprotectants or drugs for treating neurodegenerative diseases such as Parkinson's disease.

Synthesis of C-13 oxidised cuparene and herbertane sesquiterpenes via a Paternò-Büchi photocyclisation-oxetane fragmentation strategy: Total synthesis of 1,13-herbertenediol

The intramolecular Paternò-Büchi reaction of 5-aryl-4,4-dimethyl-hex-5-enals has been used to assemble the hindered cyclopentane skeleton of the cuparene and herbertane sesquiterpenes. Regioselective carbon-oxygen bond cleavage in the resulting oxetane is