58888-90-7

Usage

InChI:InChI=1/C11H22O2/c1-3-5-7-10(8-6-4-2)9-11(12)13/h10H,3-9H2,1-2H3,(H,12,13)

Upstream product

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Relevant academic research and scientific papers

Sterically Directed Conjugate Addition Reactions of Unsaturated Esters

Unsaturated esters of 2,6-di-tert-butyl-4-meethoxyphenol undergo conjugate addition reactions with a variety of organolithium reagents.Oxidation of adducts with ceric ammonium nitrate provides substituted carboxylic acids.

RECHERCES SUR LES SUBSTANCES MESOMORPHES-IX; SMECTIQUES "FOURCHUS". ORGANISATION MOLECULAIRE DANS LES PHASES SMECTIQUES

The synthesis and the mesomorphic properties of new branched smectogenic A derivatives of fluorene are described.The observation that branched chain compounds from a smectic A phase allows conclusions to be drawn on molecular arrangements in smectic A layers.

Research in dipropylacetic series. XII. Aliphatic ramified acids and alcohols with anticonvulsant activity

Previous results obtained about 2 propyl pentanoic acid (dipropylacetic or DPA) have been extended to other dialkylalkanoic acids having less than 14 carbon atoms and to some of their precursors (alcohols) or derivatives (amides). The effect of lengthening the chain bonding between the carbon bearing the two alkyl chains and the functional carbon on about 50 molecules is discussed. The anticonvulsant activity's length and strength often increases when lengthening that chain.