58344-27-7

Usage

Chemical Properties

Yellow Solid

Uses

Intermediate in the preparation of Stiripentol metabolites.

InChI:InChI=1/C14H18O3/c1-14(2,3)13(16)8-6-10-5-7-11(15)12(9-10)17-4/h5-9,15H,1-4H3/b8-6+

Upstream product

• 75-97-8 3,3-dimethyl-butan-2-one 
• 121-33-5 vanillin 
• 91471-08-8 3-methoxy-4-(tetrahydropyran-2-yloxy)benzaldehyde 

Downstream Products

• 106174-97-4 1-(4-hydroxy-3-methoxyphenyl)-4,4-dimethylpentan-3-one 
• 58344-42-6 4-((E)-3-Hydroxy-4,4-dimethyl-pent-1-enyl)-2-methoxy-phenol 

Relevant academic research and scientific papers

Selective hydrogenation of conjugated unsaturated ketones containing a hydroxyaryl substituent in the β-position

A high selectivity was achieved in the Ni2B-catalyzed hydrogenation of α,β-unsaturated ketones containing a hydroxyaryl (phenolic) substituent in the β-position. The developed hydrogenation procedure was used to synthesize natural compounds of the phenylpropane series and their structural analogs.

COMPOSITIONS AND METHODS FOR THE TREATMENT OF EPILEPSY AND NEUROLOGIC DISEASES

The invention relates to the compounds of formula I or its pharmaceutical acceptable salts, as well as polymorphs, solvates, enantiomers, stereoisomers and hydrates thereof. The pharmaceutical compositions comprising an effective amount of compounds of fo

Central nervous system agents: new α ethylenic alcohols

The study of the sedative and anticonvulsive properties of a series of 1-alkoxyaryl 3-alkyl 1-alkene 3-ol and of the ketones from which they originate enabled us to select five compounds whose psychopharmacological effects were further studied. One of these compounds, 4,4-dimethyl 1-(3,4-methylene dioxy phenyl) 1-pentene 3-ol owns important anticonvulsive and sedative properties.