111220-81-6

Basic information

• Product Name: methyl 2-(p-chlorophenylsulphinyl)-4-methyl-3-(4-methylpiperidino)pentanoate
• CAS NO: 111220-81-6
• Molecular Weight: 385.955
• Mol File: 111220-81-6.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: methyl 2-(p-chlorophenylsulphinyl)-4-methyl-3-(4-methylpiperidino)pentanoate(CAS DataBase Reference)
• NIST Chemistry Reference: methyl 2-(p-chlorophenylsulphinyl)-4-methyl-3-(4-methylpiperidino)pentanoate(111220-81-6)
• EPA Substance Registry System: methyl 2-(p-chlorophenylsulphinyl)-4-methyl-3-(4-methylpiperidino)pentanoate(111220-81-6)

Safety Data

• Hazardous Substances Data: 111220-81-6(Hazardous Substances Data)

Upstream product

• 111220-78-1 methyl 2-(p-chlorophenylsulphinyl)-3-hexanethyleneimino-3-phenylpropanoate 
• 102714-50-1 methyl 2-(p-chlorophenylsulphinyl)-3-phenyl-3-piperidinopropanoate 
• 102714-51-2 methyl 2-(p-chlorophenylsulphinyl)-3-(2-methylpiperidino)-3-phenylpropanoate 
• 111220-77-0 methyl 2-(p-chlorophenylsulphinyl)-3-(3-methylpiperidino)-3-phenylpropanoate 
• 111220-80-5 methyl 2-(p-chlorophenylsulphinyl)-4-methyl-3-(2-methylpiperidino)pentanoate 
• 111220-81-6 methyl 2-(p-chlorophenylsulphinyl)-4-methyl-3-(4-methylpiperidino)pentanoate 
• 102714-52-3 methyl 2-(p-chlorophenylsulphinyl)-4-methyl-3-piperidinopentanoate 
• 626-58-4 4-methylpiperidin 
• 73281-90-0 methyl 4-chlorophenylsulfinylacetate 
• 78-84-2 isobutyraldehyde 
• 102714-49-8 methyl 2-(p-chlorophenylsulphinyl)-3-phenyl-3-pyrrolidinopropanoate 

Downstream Products

• 102714-43-2 (E)-methyl 2-(p-chlorophenylsulphinyl)hex-2-enoate 
• 111220-71-4 (E)-methyl 2-(p-chlorophenylsulphinyl)non-2-enoate 
• 102714-49-8 methyl 2-(p-chlorophenylsulphinyl)-3-phenyl-3-pyrrolidinopropanoate 
• 111220-79-2 methyl 2-(p-chlorophenylsulphinyl)-3-(4-methoxyphenyl)-3-piperidinopropanoate 
• 90381-85-4 (E)-methyl 2-(p-chlorophenylsulphinyl)-4-methylpent-2-enoate 
• 111274-05-6 (Z)-methyl 2-(p-chlorophenylsulphinyl)-3-phenylprop-2-enoate 
• 102714-42-1 (E)-methyl 2-(p-chlorophenylsulphinyl)-3-phenylprop-2-enoate 
• 102714-52-3 methyl 2-(p-chlorophenylsulphinyl)-4-methyl-3-piperidinopentanoate 
• 102714-52-3 methyl 2-(p-chlorophenylsulphinyl)-4-methyl-3-piperidinopentanoate 
• 111220-81-6 methyl 2-(p-chlorophenylsulphinyl)-4-methyl-3-(4-methylpiperidino)pentanoate 
• 111220-81-6 methyl 2-(p-chlorophenylsulphinyl)-4-methyl-3-(4-methylpiperidino)pentanoate 
• 111220-80-5 methyl 2-(p-chlorophenylsulphinyl)-4-methyl-3-(2-methylpiperidino)pentanoate 
• 111220-80-5 methyl 2-(p-chlorophenylsulphinyl)-4-methyl-3-(2-methylpiperidino)pentanoate 
• 111220-77-0 methyl 2-(p-chlorophenylsulphinyl)-3-(3-methylpiperidino)-3-phenylpropanoate 

Relevant articles and documents

Stereochemistry in the Knoevenagel Reaction of Methyl Arylsulphinylacetate and Aldehydes

The stereochemistry of the mechanism of the amine-catalyzed Knoevenagel reaction has been studied.Simple treatment of methyl arylsulphinylacetate (1) and aldehydes (2) with a catalytic amount of a secondary amine produced thermodynamically stable E-alkene