379395
Ethyl 1-piperidineacetate
98%
Synonym(s):
Piperidin-1-ylacetic acid ethyl ester
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About This Item
Empirical Formula (Hill Notation):
C9H17NO2
CAS Number:
Molecular Weight:
171.24
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
assay
98%
form
liquid
refractive index
n20/D 1.453 (lit.)
bp
109-111 °C/25 mmHg (lit.)
density
0.984 g/mL at 25 °C (lit.)
SMILES string
CCOC(=O)CN1CCCCC1
InChI
1S/C9H17NO2/c1-2-12-9(11)8-10-6-4-3-5-7-10/h2-8H2,1H3
InChI key
LXZHLNWWDDNIOJ-UHFFFAOYSA-N
General description
Ethyl 1-piperidineacetate (Piperidin-1-ylacetic acid ethyl ester) is an α-amino acid ethyl ester derivative. Thermal decomposition of ethyl 1-piperidineacetate in gas phase has been studied by ab initio theoretical methods.[1] The kinetics of gas-phase decomposition of ethyl 1-piperidineacetate to the corresponding α-amino acid derivative and ethylene over the temperature range of 360-430°C and pressure range of 26-86Torr has been investigated.[2] Alkylation reaction of ethyl 1-piperidineacetate with ethyl bromoacetate in absolute ethanol has been reported to obey second order kinetics.[3]
Application
Reactant for synthesis of:
Nicotinic acid receptor agonists for treatment of dyslipidemia
1-Alkylcyclanols with side chain functions
Benzhydrylamides for pharmacochemical studies
Reactant for:
Elimination reactions
Hydrogenation of esters to alcohols
Nicotinic acid receptor agonists for treatment of dyslipidemia
1-Alkylcyclanols with side chain functions
Benzhydrylamides for pharmacochemical studies
Reactant for:
Elimination reactions
Hydrogenation of esters to alcohols
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
10 - Combustible liquids
wgk_germany
WGK 3
flash_point_f
195.8 °F - closed cup
flash_point_c
91 °C - closed cup
ppe
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
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Theoretical study of the gas-phase decomposition of neutral α-amino acid ethyl esters. Part 2-Elimination of ethyl picolinate and ethyl 1-methylpipecolinate.
Notario R, et al.
Journal of Physical Organic Chemistry, 16(3), 166-174 (2003)
Alkylation of N-carbethoxy tertiary amines with ethyl bromoacetate.
Duty RC and Gurnea RL.
The Journal of Organic Chemistry, 35(6), 1800-1802 (1970)
The mechanism of neutral amino acid decomposition in the gas phase. The elimination kinetics of N, N-dimethylglycine ethyl ester, ethyl 1-piperidineacetate, and N, N-dimethylglycine.
Ensuncho A, et al.
International Journal of Chemical Kinetics, 33(8), 465-471 (2001)
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