Ethyl piperidine-2-carboxylate

Suppliers

Names

[ Name ]:
Ethyl piperidine-2-carboxylate

[Synonym ]:
2-Piperidinecarboxylic acid, ethyl ester, hydrochloride (1:1)
MFCD00134518
Ethyl 2-piperidinecarboxylate hydrochloride (1:1)
ethyl piperidine-2-carboxylate,hydrochloride
Ethyl piperidine-2-carboxylate hydrochloride (1:1)
Ethyl piperidine-2-carboxylate

Chemical & Physical Properties

[ Boiling Point ]:
254ºC at 760 mmHg

[ Melting Point ]:
211-213ºC

[ Molecular Formula ]:
C₈H₁₆ClNO₂

[ Molecular Weight ]:
193.671

[ Flash Point ]:
107.4ºC

[ Exact Mass ]:
193.086960

[ PSA ]:
38.33000

[ LogP ]:
1.82240

MSDS

Click to get detail MSDS

Safety Information

[ Symbol ]:

GHS05

[ Signal Word ]:
Danger

[ Hazard Statements ]:
H318

[ Precautionary Statements ]:
P280-P305 + P351 + P338

[ Personal Protective Equipment ]:
dust mask type N95 (US);Eyeshields;Gloves

[ Hazard Codes ]:
Xi:Irritant;

[ Risk Phrases ]:
R41

[ Safety Phrases ]:
S26-S36/39

[ RIDADR ]:
NONH for all modes of transport

[ HS Code ]:
2933399090

Synthetic Route

Click to get detail synthetic route

Precursor & DownStream

Precursor

DownStream

Customs

[ HS Code ]: 2933399090

[ Summary ]:
2933399090. other compounds containing an unfused pyridine ring (whether or not hydrogenated) in the structure. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

Articles

Syntheses of benzoquinolizidine and benzoindolizidine derivatives as anti-amnesic agents.

Bioorg. Med. Chem. 7 , 1637-1646, (1999)

Tacrine, one of the drugs available for Alzheimer's disease based on the cholinergic approach, suffers from considerable toxicity. Many analogues of tacrine have been prepared which retain the pharmac...

Pipecolic acid derivatives as small-molecule inhibitors of the Legionella MIP protein.

J. Med. Chem. 54 , 277-283, (2011)

The macrophage infectivity potentiator (MIP) protein is a major virulence factor of Legionella pneumophila, the causative agent of Legionnaires' disease. MIP belongs to the FK506-binding proteins (FKB...

G. A. Gevorgyan, et al.,

Khim.-Farm. Zh. 37 , 152-154, (2003)