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Ethyl pipecolinate_Molecular_structure_CAS_15862-72-3)
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Ethyl pipecolinate

Catalog No. 198803 Name Sigma Aldrich
CAS Number 15862-72-3 Website http://www.sigmaaldrich.com
M. F. C8H15NO2 Telephone 1-800-521-8956
M. W. 157.2102 Fax
Purity 98% Email
Storage Chembase ID: 70242

SYNONYMS

Title
2-哌啶甲酸乙酯
IUPAC name
ethyl piperidine-2-carboxylate
IUPAC Traditional name
ethyl piperidine-2-carboxylate
Synonyms
NSC 49360
2-(Ethoxycarbonyl)piperidine
DL-Pipecolic acid ethyl ester
Ethyl 2-piperidinecarboxylate
2-哌啶羧酸乙酯

DATABASE IDS

CAS Number 15862-72-3
EC Number 239-990-6
MDL Number MFCD00005980
PubChem SID 24851881

PROPERTIES

Empirical Formula (Hill Notation) C8H15NO2
Purity 98%
Boiling Point 216-217 °C(lit.)
Density 1.006 g/mL at 25 °C(lit.)
Flash Point 46 °C
Flash Point 114.8 °F
Refractive Index n20/D 1.456(lit.)
GHS Pictograms GHS02
GHS Pictograms GHS07
GHS Signal Word Warning
GHS Hazard statements H226-H315-H319-H335
European Hazard Symbols Irritant Irritant (Xi)
MSDS Link Download
Personal Protective Equipment Eyeshields, Faceshields, full-face respirator (US), Gloves, multi-purpose combination respirator cartridge (US), type ABEK (EN14387) respirator filter
GHS Precautionary statements P261-P305 + P351 + P338
RID/ADR UN 1993 3/PG 3
Risk Statements 10-36/37/38
Safety Statements 26-36
Storage Temperature 2-8°C
Hazard Class 3
UN Number 1993
Packing Group 3
German water hazard class 3

DETAILS

Description (English)
Packaging
5, 25 g in glass bottle
Application
Reactant for: Combinatorial chemistry with hydrazones1 Swift hydroamination2 Synthesis of HCV NS5B polymerase inhibitors3 Preparation of selective androgen receptor modulators4 Decarbonylative arylation at sp3 carbon centers5 Synthesis of quinoline derivatives as selective a2C-adrenoceptor antagonists6
Description (简体中文)
包装
5, 25 g in glass bottle
Application
Reactant for: Combinatorial chemistry with hydrazones1 Swift hydroamination2 Synthesis of HCV NS5B polymerase inhibitors3 Preparation of selective androgen receptor modulators4 Decarbonylative arylation at sp3 carbon centers5 Synthesis of quinoline derivatives as selective a2C-adrenoceptor antagonists6

REFERENCES