1193-93-7

Upstream product

• 108-91-8 cyclohexylamine 
• 75-07-0 acetaldehyde 
• 64-17-5 ethanol 
• 14668-82-7 vinyl isocyanide 
• 74-86-2 acetylene 

Downstream Products

• 10108-56-2 N-butylcyclohexylamine 
• 37414-73-6 4-(2-cyanoethyl)-4-cyclohexyliminomethylheptane-1,7-dinitrile 
• 27719-16-0 N-vinyl-N-cyclohexylcarbamyl chloride 
• 1197-52-0 N-cyclohexylbutylideneamine 
• 30930-83-7 hexanal cyclohexylimine 
• 14609-19-9 C₁₆H₂₉NO 
• 14035-50-8 2-<1-Hydroxy-cyclohexyl>-aethyliden-cyclohexylamin 
• 30930-85-9 Phenyl-3-benzyl-2-propionaldehyd-cyclohexylimin 
• 22859-80-9 2-benzyl-3-phenylpropionaldehyde 
• 2100-17-6 4-pentenal 
• 1200-02-8 cyclohexyl-pent-4-enylidene-amine 
• 18498-59-4 4-pentyn-1-al 
• 30930-81-5 cyclohexyl-pent-4-ynylidene-amine 
• 85336-14-7 Cyclohexyl-[1,4,4-trimethyl-pent-2-yn-(Z)-ylidene]-amine 

Relevant academic research and scientific papers

Synthesis of imines from amines in aliphatic alcohols on Pd/ZrO2 catalyst under ambient conditions

Synthesis of imines from amines and aliphatic alcohols (C 1-C6) in the presence of base on supported palladium nanoparticles has been achieved for the first time. The catalytic system shows high activity and selectivity in open air at room temperature.

PNP pincer osmium polyhydrides for catalytic dehydrogenation of primary alcohols

This paper reports the synthesis, structure, and properties of a series of PNP pincer complexes of osmium OsH3Cl[HN(C2H 4PiPr2)2] (1), OsH 3[N(C2H4PiPr2) 2] (2), OsH4[HN(C2H4P iPr2)2] (3), and OsH2(PMe 3)[HN(C2H4PiPr2) 2] (4). The tetrahydride 3 operates as an efficient catalyst at 0.1 mol% loading for the reactions of amination and dehydrogenative coupling of primary alcohols, producing secondary amines and symmetrical esters, respectively. The catalyst 3 is distinguished by outstanding stability, and it can be used in an aqueous environment at temperatures as high as 200 °C. The Royal Society of Chemistry 2011.

PROCESS FOR PRODUCING QUINOLINE COMPOUND

By a production method of a quinoline compound represented by the formula (I), which comprises reacting quinolinecarbaldehyde represented by the formula (II) with an imine compound represented by the formula (III) and then subjecting the resulting compoun

Synthesis of the 3-methylene-2-vinyltetrahydropyran unit; the hallmark of the sesquiterpene, hodgsonox

(Chemical Equation Presented) The synthesis of some simple compounds containing the previously unreported 3-methylene-2-vinyltetrahydropyran system, a unique feature of the liverwort metabolite, hodgsonoxis reported. Key features are the creation of an ac

Nitrogen-heterocyclic compound and process for production thereof

A nitrogen-heterocyclic compound is provided which is represented by General Formula (1): where R1and R2are independently hydrogen, an alkyl group, an aryl group, or a heteroaryl group; R3is hydrogen or an aryl group; Rsu

Synthesis of 5,7-Dichloro-2H-1-benzopyran-2-ol

The reaction of 4,6-dichloro-2-(methylthiomethoxy)cinnamaldehyde (3) or 4,6-dichloro-2-hydroxycinnamaldehyde (5) with mercuric chloride in hot aqueous acetonitrile gave 5,7-dichloro-2H-1-benzopyran-2-ol (4) in good yield.