38376-28-2

Usage

InChI:InChI=1/C11H24O2/c1-10(7-9-12)6-5-8-11(2,3)13-4/h10,12H,5-9H2,1-4H3

Upstream product

• 67-56-1 methanol 
• 141-11-7 3,7-dimethyl-7-octen-1-ol acetate 
• 106-22-9 Citronellol 
• 125161-79-7 1-acetoxy-5-bromo-3-methylpentane 
• 3613-30-7 7-methoxy-3,7-dimethyloctanal 
• 443792-14-1 ethyl 2-acetyl-7-acetoxy-5-methylheptanoate 
• 63539-99-1 8-acetoxy-6-methyloctan-2-one 

Downstream Products

• 3613-30-7 7-methoxy-3,7-dimethyloctanal 
• 65733-16-6 (S)-methoprene 

Relevant academic research and scientific papers

Hydroalkoxylation of non-activated olefins catalysed by Lewis superacids in alcoholic solvents: an eco-friendly reaction

Lewis superacids such as tin(IV) triflate catalyse the intermolecular addition of primary alcohols to non-activated olefins under mild conditions.

Universal approach to the synthesis of juvenoid hydroprene and methoprene from 4-methyltetrahydropyran

A universal approach to the synthesis of juvenoid hydroprene and methoprene was developed on the basis of monoalkylation of acetoacetate by 1-acetoxy-5-bromo-3-methylpentane, the product of acidic decyclization of 4-methyltetrahydropyran.

Phenolic ethers

Novel phenyl derivatives of formula I useful for the control of insects and novel intermediates.

Novel benzofuranyl pest retardants

Alkyl ethers of 2,3-dihydrobenzofuran where the alkyl chain may contain branched chains, unsaturated bonds, epoxy bridges, and may be substituted with halo, alkoxy, lower alkenyloxy, or lower alkynyloxy substituents useful in killing and preventing the proliferation of insects and other pests by upsetting their hormone balance.