113795-41-8

Upstream product

• 5581-75-9 6-phenylhexanic acid 
• 637-59-2 1-Bromo-3-phenylpropane 
• 374754-93-5 (9-BBN)(CH₂)3(p-anisyl) 
• 21389-46-8 6-phenylhexanoyl chloride 
• 113795-40-7 1-(4-methoxyphenyl)-6-phenylhexan-1-one 

Downstream Products

• 113795-46-3 4-(6-Phenyl-hexyl)-phenol 
• 113795-08-7 2,2-Dimethyl-5-[4-(6-phenyl-hexyl)-phenoxy]-pentanoic acid 
• 113795-32-7 1-(3-Bromo-propoxy)-4-(6-phenyl-hexyl)-benzene 

Relevant academic research and scientific papers

High yielding alkylations of unactivated sp3 and sp2 centres with alkyl-9-BBN reagents using an NHC-based catalyst: Pd-PEPPSI-IPr

High yielding, room temperature cross couplings of unactivated alkyl bromides and aryl bromides/chlorides with alkyl-9-BBN reagents has been achieved using an NHC-based catalyst (Pd-PEPPSI-IPr) via a general, functional-group tolerant and easily implemented protocol. The Royal Society of Chemistry.

Synthesis and Hypolipidemic Activity of 2-Substituted Isobutyric Acid Derivatives

A series of 2-substituted isobutyric acid derivatives have been synthesized and evaluated as hypolipidemic agents.Compounds 11 and 20 were found to decrease the level of plasma total cholesterol in experimental hyperlipidemic rats to a greater extent than clofibrate (CF) and to increase the level of plasma high-density lipoprotein cholesterol to the same extent as gemfibrozil (GF).Increase in liver weight caused by these compounds were less than those with CF and GF.