N-Formylpiperidine

N-Formylpiperidine
  • CAS No.:2591-86-8
Other grades of this product :
N-Formylpiperidine Basic information
Product Name:N-Formylpiperidine
Synonyms:1-formyl-piperidin;1-Piperidinecarbaldehyde;N-Formylpiperdine;N-Formylpiperidin;1-Formylpiperidine,99%;N-Carbaldehyde piperidine;N-Formylpiperidine for synthesis;N-ForMylpiperidine, 99% 250ML
CAS:2591-86-8
MF:C6H11NO
MW:113.16
EINECS:219-986-0
Product Categories:Piperidine
Mol File:2591-86-8.mol
N-Formylpiperidine Chemical Properties
Melting point -31 °C
Boiling point 222 °C(lit.)
density 1.019 g/mL at 25 °C(lit.)
vapor pressure 0.1 mm Hg ( 25 °C)
refractive index n20/D 1.484(lit.)
Fp 197 °F
storage temp. Store below +30°C.
form Liquid
pka-0.44±0.20(Predicted)
Specific Gravity1.02
color Clear colorless to slightly yellow
Water Solubility freely soluble
BRN 107697
CAS DataBase Reference2591-86-8(CAS DataBase Reference)
NIST Chemistry Reference1-Piperidinecarboxaldehyde(2591-86-8)
EPA Substance Registry SystemN-Formylpiperidine (2591-86-8)
Safety Information
Hazard Codes Xn,Xi
Risk Statements 21/22-36/37/38
Safety Statements 26-36/37-36
RIDADR UN 2810 6.1/PG 3
WGK Germany 3
RTECS TN0380000
TSCA Yes
HazardClass 6.1(b)
PackingGroup III
HS Code 29333999
MSDS Information
ProviderLanguage
N-Formylpiperidine English
SigmaAldrich English
ACROS English
ALFA English
N-Formylpiperidine Usage And Synthesis
DescriptionThis simple piperidine base has recently been discovered in the oxygenated fraction from Piper nigrum. The structure has been elucidated from chemical and spectroscopic data.
Chemical PropertiesCLEAR COLOURLESS TO SLIGHTLY YELLOW LIQUID
UsesSolvent for polar and nonpolar compounds, as well as many high polymers; gas absorption; plastics modifiers.
UsesReactant for:
  • Direct amidation of azoles with formamides via metal-free C-H activation in the presence of tert-butyl perbenzoate
  • Vilsmeier-type reactions of pyrazoles with amides in the presence of phosphorous oxychloride
  • CO-free aminocarbonylation of N-substituted formamides with aryl iodides/bromides catalyzed by palladium acetate and Xantphos for synthesis of arylamides
  • Synthesis of alternating copolymers for organic photovoltaic applications
  • One-pot double functionalization of π-deficient heterocyclic lithium reagents
  • Synthesis of thermally stable piezofluorochromic aggregation-induced emission compounds
Synthesis Reference(s)Chemical and Pharmaceutical Bulletin, 42, p. 1655, 1994 DOI: 10.1248/cpb.42.1655Synthetic Communications, 20, p. 447, 1990 DOI: 10.1080/00397919008052787
ReferencesDebrauwere, Verzale, Bull. Soc. Chim. Belg., 84, 167 (1975)

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