66893-75-2

Basic information

• Product Name: 1-Piperidinecarboxylic acid, 2-methoxy-, phenylmethyl ester
• CAS NO: 66893-75-2
• Molecular Formula: C14H19NO3
• Molecular Weight: 249.31
• Mol File: 66893-75-2.mol
• Article Data: 9

Chemical Properties

• CAS DataBase Reference: 1-Piperidinecarboxylic acid, 2-methoxy-, phenylmethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Piperidinecarboxylic acid, 2-methoxy-, phenylmethyl ester(66893-75-2)
• EPA Substance Registry System: 1-Piperidinecarboxylic acid, 2-methoxy-, phenylmethyl ester(66893-75-2)

Safety Data

• Hazardous Substances Data: 66893-75-2(Hazardous Substances Data)

Upstream product

• 67-56-1 methanol 
• 1227635-49-5 α-benzyl-N-benzyloxycarbonylpiperidine 
• 106412-35-5 N-benzyloxycarbonyl-2-piperidone 
• 69622-67-9 benzyl 2-hydroxypiperidine-1-carboxylate 
• 3742-91-4 N-(benzyloxycarbonyl)piperidine 

Downstream Products

• 73269-82-6 2-(5-Fluoro-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-piperidine-1-carboxylic acid benzyl ester 
• 80953-71-5 3,4,5,6,5',6'-Hexahydro-2H,4'H-[2,3']bipyridinyl-1,1'-dicarboxylic acid dibenzyl ester 
• 69622-67-9 benzyl 2-hydroxypiperidine-1-carboxylate 
• 68471-58-9 1-(benzyloxycarbonyl)-1,2,3,4-tetrahydropyridine 
• 1227635-84-8 α-(1-myristylallyl)-N-benzyloxycarbonylpiperidine 
• 1227635-49-5 α-benzyl-N-benzyloxycarbonylpiperidine 
• 86827-08-9 benzyl 3-(2-methoxy-2-oxoethyl)piperidine-1-carboxylate 
• 1034844-81-9 benzyl 5-(methoxymethyl)-3,4-dihydropyridine-1(2H)-carboxylate 
• 493009-89-5 α-allyl-N-benzyloxycarbonylpiperidine 
• 1010732-19-0 2,3,4-triacetoxy-piperidine-1-carboxylic acid benzyl ester 
• 799805-78-0 6-methoxy-3,6-dihydro-2H-pyridine-1-carboxylic acid benzyl ester 

Relevant articles and documents

Fragment-oriented synthesis: β-elaboration of cyclic amine fragments using enecarbamates as platform intermediates

A strategy for the β-sp3 functionalisation of cyclic amines is described. Regioselective conversion of protected amines to enecarbamates is achieved through electrochemical oxidation; these intermediates can be derivatised by functionalised alkyl halides under photoredox catalysis. The potential of the methods is highlighted by direct growth of a DCP2B-binding fragment. This journal is

Diastereoselective synthesis of 3-fluoro-2-substituted piperidines and pyrrolidines

A facile procedure for synthesis of trans-3-fluoro-2-substituted piperidines by utilizing electrophilic fluorination of cyclic enamines and Lewis acid mediated nucleophilic substitution has been developed. Also, optically active trans-2-allyl-3-fluorinate

Stereoselective synthesis of 3-deoxy-piperidine iminosugars from l-lysine

A new method using electrochemical oxidation and/or OsO4 oxidation has been used for the stereoselective synthesis of 2,3,6-trihydroxylated (5S)-piperidine derivatives. The electrochemical method was successively used for the conversion of N-pr