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N-Methylpiperidine

Catalog No. M72609 Name Sigma Aldrich
CAS Number 626-67-5 Website http://www.sigmaaldrich.com
M. F. C6H13N Telephone 1-800-521-8956
M. W. 99.17412 Fax
Purity 99% Email
Storage Chembase ID: 76875

SYNONYMS

Title
N-甲基哌啶
IUPAC name
1-methylpiperidine
IUPAC Traditional name
N-methylpiperidine

DATABASE IDS

EC Number 210-959-9
MDL Number MFCD00006491
PubChem SID 24897150
CAS Number 626-67-5
Beilstein Number 1073

PROPERTIES

Empirical Formula (Hill Notation) C6H13N
Purity 99%
Boiling Point 106-107 °C(lit.)
Density 0.816 g/mL at 25 °C(lit.)
Flash Point 3 °C
Flash Point 37.4 °F
Refractive Index n20/D 1.4378(lit.)
GHS Pictograms GHS02
GHS Pictograms GHS05
GHS Signal Word Danger
GHS Hazard statements H225-H314
European Hazard Symbols Flammable Flammable (F)
European Hazard Symbols Corrosive Corrosive (C)
MSDS Link Download
Personal Protective Equipment Faceshields, full-face respirator (US), Gloves, Goggles, multi-purpose combination respirator cartridge (US), type ABEK (EN14387) respirator filter
GHS Precautionary statements P210-P280-P305 + P351 + P338-P310
RID/ADR UN 2399 3/PG 2
Risk Statements 11-34
RTECS TN1225000
Safety Statements 16-26-36/37/39-45
Hazard Class 3
UN Number 2399
Packing Group 2
German water hazard class 3

DETAILS

Description (English)
Packaging
100, 500 mL in glass bottle
Application
Reactant for:
• sp3 C-H Bond activation with ruthenium(II) catalysts and C(3)-alkylation of cyclic amines1
• One-pot synthesis of Z-cinnamic acids2Reactant for synthesis of:
• Unsymmetrical ureas3
• Antibacterial imidazolium, pyrrolidinium, and piperidinium salts4
• C1-C16 segment of goniodomin A via palladium-catalyzed organostannane thioester coupling5
• Multi-targeted inhibitors of insulin-like growth factor-1 receptor and members of ErbB-family receptor kinases6
Description (简体中文)
包装
100, 500 mL in glass bottle
Application
Reactant for:
• sp3 C-H Bond activation with ruthenium(II) catalysts and C(3)-alkylation of cyclic amines1
• One-pot synthesis of Z-cinnamic acids2Reactant for synthesis of:
• Unsymmetrical ureas3
• Antibacterial imidazolium, pyrrolidinium, and piperidinium salts4
• C1-C16 segment of goniodomin A via palladium-catalyzed organostannane thioester coupling5
• Multi-targeted inhibitors of insulin-like growth factor-1 receptor and members of ErbB-family receptor kinases6

REFERENCES