7032-62-4

Basic information

• Product Name: METHYL 3-PHENYL-3-(PIPERIDIN-1-YL)PROPANOATE
• Synonyms: beta-phenyl-1-piperidinepropionicacidmethylester;beta-phenyl-1-piperidinepropionicacimethylester;METHYL 3-PHENYL-3-(PIPERIDIN-1-YL)PROPANOATE
• CAS NO: 7032-62-4
• Molecular Formula: C₁₅H₂₁NO₂
• Molecular Weight: 247.33
• Mol File: 7032-62-4.mol
• Article Data: 6

Chemical Properties

• Boiling Point: 346.4°C at 760 mmHg
• Flash Point: 114.4°C
• Appearance: /
• Density: 1.077g/cm³
• Vapor Pressure: 5.76E-05mmHg at 25°C
• Refractive Index: 1.534
• CAS DataBase Reference: METHYL 3-PHENYL-3-(PIPERIDIN-1-YL)PROPANOATE(CAS DataBase Reference)
• NIST Chemistry Reference: METHYL 3-PHENYL-3-(PIPERIDIN-1-YL)PROPANOATE(7032-62-4)
• EPA Substance Registry System: METHYL 3-PHENYL-3-(PIPERIDIN-1-YL)PROPANOATE(7032-62-4)

Safety Data

• Hazardous Substances Data: 7032-62-4(Hazardous Substances Data)

Usage

InChI:InChI=1/C15H21NO2/c1-18-15(17)12-14(13-8-4-2-5-9-13)16-10-6-3-7-11-16/h2,4-5,8-9,14H,3,6-7,10-12H2,1H3

Upstream product

• 110-89-4 piperidine 
• 77086-38-5 ketene t-butyldimethylsilyl methyl acetal 
• 100-52-7 benzaldehyde 
• 3646-50-2 3-Amino-3-phenylpropionic acid 
• 111-24-0 1,5-dibromo-pentane 
• 22838-46-6 methyl 3-amino-3-phenylpropionate hydrochloride 
• 103-26-4 Methyl cinnamate 
• 108-88-3 toluene 

Relevant articles and documents

B(OMe)3 as a nonacidic iminium ion generator in Mannich- and Ugi-type reactions

Mannich-type reactions of aldehydes with secondary amines and a ketene silyl acetal were promoted by trimethoxyborane in DMSO to afford the corresponding β-amino esters in good yields. B(OMe)3 also promoted Ugi-type reactions of aldehydes with

Cu(acac)2 immobilized in ionic liquids: A recoverable and reusable catalytic system for aza-Michael reactions

Copper(II) acetylacetonate immobilized in ionic liquids efficiently catalyzes the aza-Michael reaction of amines with α,β-unsaturated carbonyl compounds to produce the corresponding β-amino carbonyl compounds with great alacrity in excellent yields. The reactions are far more facile than those reported earlier. The recovered ionic liquid phase containing the copper catalyst can be reused for several cycles with consistent activity.

Air- and moisture-stable cationic (diphosphine)palladium(II) complexes as hydroamination catalysts X-ray crystal structures of two complexes

A series of cationic (diphosphine)palladium(II) complexes have been prepared and fully characterized, including two crystal structures. These complexes were evaluated as catalysts for the hydroamination of acyclic alkenes. The reactivity of the catalysts is dependent on the nature of the diphosphine ligand and the substituents on the amine and alkene substrates.