Interesting facts
Interesting Facts about Ethyl Piperidine-2-Carboxylate
Ethyl piperidine-2-carboxylate is an intriguing compound that captures the interest of both organic chemists and pharmacologists. This compound is notable for its structural features and potential applications in medicinal chemistry. Here are some interesting points about ethyl piperidine-2-carboxylate:
- Structural Significance: The piperidine ring is a six-membered heterocyclic structure featuring one nitrogen atom. This ring system is known for its effectiveness in various chemical reactions, making it a valuable building block in organic synthesis.
- Versatile Intermediate: Ethyl piperidine-2-carboxylate acts as an important intermediate in the synthesis of a variety of other compounds, particularly in the development of pharmaceuticals. Its ability to participate in nucleophilic substitution and other reactions opens doors to a wide array of complex molecules.
- Pharmacological Potential: Compounds containing the piperidine structure have been shown to possess diverse biological activities. Research indicates that derivatives of this compound may exhibit properties beneficial in treating conditions such as hypertension, pain, and various neurodegenerative diseases.
- Applications in Synthesis: Aside from medicinal chemistry, ethyl piperidine-2-carboxylate is utilized in the synthesis of agrochemicals and dyes, showcasing its versatility across different fields of chemical research.
- Chemical Stability: Ethyl piperidine-2-carboxylate is relatively stable under standard conditions, which is advantageous for laboratory handling and storage. This stability allows chemists to work with it confidently in various reactions.
The study of ethyl piperidine-2-carboxylate exemplifies the fascinating interplay between structure and function in organic chemistry. As researchers continue to explore its properties and potential applications, this compound remains a staple in the toolkit of synthetic chemists.
Synonyms
15862-72-3
Ethyl piperidine-2-carboxylate
Ethyl 2-piperidinecarboxylate
EINECS 239-990-6
DTXSID501307286
NSC 49360
DTXCID20836045
239-990-6
Ethyl pipecolinate
Ethyl Pipecolate
2-Piperidinecarboxylic acid, ethyl ester
Pipecolic Acid Ethyl Ester
Pipecolinic Acid Ethyl Ester
MFCD00005980
ethylpipecolinate
2-Piperidinecarboxylic Acid Ethyl Ester
Ethyl pipecolinate, 98%
ChemDiv3_014133
2-(ethoxycarbonyl)piperidine
DL-Pipecolic acid ethyl ester
SCHEMBL135813
SCHEMBL234450
ethyl 2-piperidine carboxylate
ethyl 2-piperidine-carboxylate
Ethyl (2-piperidyl)carboxylate
SCHEMBL6583980
2-ethoxycarbonylhexahydropyridine
Ethyl 2-piperidinecarboxylate #
SZIKRGHFZTYTIT-UHFFFAOYSA-
HMS1513C09
ALBB-032926
NSC49360
NSC-49360
STL304620
AKOS004911158
AC-5454
GS-4242
SB42935
SB45959
SB46814
IDI1_029931
NCGC00171022-01
CS-0043929
E0837
NS00054097
ST50824636
EN300-34172
PK04_096187
AB00990803-01
F0001-0568
InChI=1/C8H15NO2/c1-2-11-8(10)7-5-3-4-6-9-7/h7,9H,2-6H2,1H3
Solubility of Ethyl Piperidine-2-Carboxylate
Ethyl piperidine-2-carboxylate is an intriguing compound whose solubility can be influenced by various factors, particularly its structure and the presence of functional groups. When assessing its solubility, consider the following aspects:
In summary, while ethyl piperidine-2-carboxylate may demonstrate limited solubility in water due to its hydrophobic aspects, its solubility in various organic solvents is enhanced by its polar features. It can be said that understanding the balance between hydrophobic and hydrophilic elements is key to predicting its solubility behavior. Therefore, keep in mind that solubility is not just a fixed characteristic but is influenced by a range of conditions and solute-solvent interactions.