87258-26-2

Upstream product

• 109-72-8 n-butyllithium 
• 111-71-7 heptanal 
• 110-43-0 n-pentyl methyl ketone 
• 121826-81-1 C₁₂H₂₄B^(1-)*Li⁽¹⁺⁾ 
• 142-62-1 hexanoic acid 
• 591-78-6 n-hexan-2-one 
• 693-25-4 n-pentylmagnesium bromide 
• 107-87-9 2-Pentanone 
• 111-13-7 hexyl-methyl-ketone 

Downstream Products

• 13151-35-4 5-methyldecane 

Relevant academic research and scientific papers

ALKYL PHENYL ALKANOLS, DERIVATIVES THEREOF AND DETERGENT COMPOSITIONS COMPRISING SAME

Alkyl phenyl alkanols and alkyl phenyl alkanol derivatives having the formula: wherein R is C5-C30 linear or branched alkyl, and mixtures thereof; R1 and R2 are independently selected from linear or branched C1-C6 alkylene; Q is a hydrocarbon moiety containing between one and six carbon atoms; Y1 and Y2 are hydrogen, SO3M, and mixtures thereof; the index x is from 0 to 50; the index z is from 0 to 20; and M is an alkali metal, alkaline earth metal, organic counterion, ammonium, substituted ammonium or mixtures thereof, that provide enhanced primary biodegrability elative to conventional surfactants such as alkyl phenol ethoxylates.

Methyl Group Migration in the Reactions of Alkynyltrialkylborates

It is shown that the methyl group cannot be used as a cheap, non-migrating group in the reactions of alkynyltrialkylborates with electrophiles.However, trimethylborane can be used as a methylboronating agent for alkynes, given the right choice of solvent, and this may be of use in terpene synthesis.

Chemoselective in situ Protection of Aldehydes and Ketones using Titanium Tetrakis(dialkylamides)

Titanium tetrakis(dialkylamides) are chemoselective protective agents for carbonyl compounds, so that such reactions as Grignard and aldol additions can be induced to occur at ketone groups in the presence of aldyhydes in a one-pot precedure.