15972-01-7

Usage

InChI:InChI=1/C11H20O2/c1-13-11(12)9-5-8-10-6-3-2-4-7-10/h10H,2-9H2,1H3

Upstream product

• 15971-99-0 4-cyclohex-3-enyl-butyric acid methyl ester 
• 67-56-1 methanol 
• 4441-63-8 4-cyclohexylbutanoic acid 
• 23684-13-1 4-oxo-hex-5-enoic acid methyl ester 
• 13487-63-3 4-(3-cyclohexanyl)butanoic acid 
• 16076-59-8 γ--γ-ketobuttersaeure-methylester 
• 201230-82-2 carbon monoxide 
• 2114-42-3 allylcyclohexane 

Downstream Products

• 4441-63-8 4-cyclohexylbutanoic acid 
• 693244-92-7 2-carbomethoxy-4-cyclohexyl-1,1-bis(methyl sulfanyl)but-1-ene 

Relevant academic research and scientific papers

Pd-Catalyzed Regioselective Alkoxycarbonylation of 1-Alkenes Using a Lewis Acid [SnCl2 or Ti(OiPr)4] and a Phosphine

The phosphine ligand mediated palladium catalyzed alkoxycarbonylation of alkenes was investigated with the objective of attaining good linear selectivity for the ester. The effect of various parameters such as solvents, additives, palladium precursors, CO pressures, and alkenes of various structural complexities were examined. The results revealed the importance of using a Lewis acid such as SnCl2 or Ti(OiPr)4 in combination with a monodentate ligand such CYTOP 292 or P(p-anisyl)3 to enhance the regioselectivity for the linear isomers in the range of 70-96%.

Fe2(SO4)3·4H 2O/concentrated H2SO4: An efficient catalyst for esterification

The mixed catalyst system, Fe2(SO4) 3·4H2O/concentrated H2SO4 has been applied to catalyse effectively the esterification of α,β-unsaturated acids, aliphatic acids and heterocyclic aromatic acids with ethanol and methanol.