Interesting facts
Interesting Facts about Piperidine-2-carboxylic Acid
Piperidine-2-carboxylic acid is a fascinating compound that holds a unique position in the world of organic chemistry. Here are some intriguing aspects of this compound:
- Structural Characteristics: The presence of a piperidine ring—a six-membered saturated nitrogen-containing heterocycle—gives this compound notable cyclic properties. This structure is not only interesting from a synthetic perspective but also influences its reactivity and biological activities.
- Biological Importance: Piperidine-2-carboxylic acid serves as a building block for various pharmaceuticals. Its derivatives have been studied for their potential in treating neurological disorders, showcasing its importance in medicinal chemistry.
- Synthesis Routes: The synthesis of piperidine-2-carboxylic acid often involves the modification of piperidine rings or the use of novel methods such as cyclizations, making it a subject of interest for organic synthetic chemists.
- Applications Beyond Medicine: Apart from its pharmaceutical applications, this compound is utilized in the production of agrochemicals and can serve as an intermediate in various organic reactions, highlighting its versatility.
- Fascinating Derivatives: The chemical can lead to numerous derivatives with different functional groups, which can alter its properties significantly and create compounds with varying biological activities.
- Research and Development: Ongoing research on piperidine-2-carboxylic acid aims to unlock new pathways for drug latching, making it a promising compound for future medicinal discoveries.
As scientists delve into the unique properties of piperidine-2-carboxylic acid, they continue to uncover its potential and versatility. Its role in shaping organic chemistry and medicinal applications cannot be overstated, making it a compound worthy of study in both academic and industrial settings.
Synonyms
piperidine-2-carboxylic acid
DL-Pipecolinic acid
535-75-1
Pipecolic acid
Pipecolinic acid
2-PIPERIDINECARBOXYLIC ACID
4043-87-2
DL-Pipecolic acid
pipecolate
Dihydrobaikiane
Piperolinic acid
L-PipecolicAcid
Hexahydropicolinic acid
Acide pipecolique
2-Carboxypiperidine
l(-)-pipecolinic acid
DL-Homoproline
MFCD00064347
(+/-)-Pipecolic acid
(R)-(+)-2-Piperidinecarboxylic acid
2-Pipecolinic acid
Hexahydro-2-picolinic acid
Acide pipecolique [French]
Acide piperidine-carboxylique-2
(+/-)-Pipecolinic acid
(+/-)-2-Piperidinecarboxylic Acid
83680-83-5
EINECS 208-616-3
EINECS 223-737-1
H254GW7PVV
NSC 17125
Acide piperidine-carboxylique-2 [French]
CHEBI:17964
.alpha.-Pipecolinic acid
NSC-17125
2-Piperidinecarboxylic acidd
PIPECOLIC ACID [MI]
piperidine-6-carboxylic acid
DTXSID40862144
2-Pyridine(carboxylic acid-13C1)
PIPECOLIC ACID DL-FORM [MI]
(+/-)-Piperidine-2-carboxylic acid
Pipecolic acid, L-
Pipecolic acid, (S)-(-)-
2-Piperidinecarboxylic acid, (S)-
MFCD00005981
homopipecolic acid
UNII-H254GW7PVV
Pipecolinate
Pipecolinicacid
Piperolinate
a-Pipecolinate
DL-Pipecolinate
DL-Pipecolate
MFCD00064346
pipecolic acid, (+,-)-isomer
alpha-Pipecolinate
Hexahydropicolinate
a-Pipecolinic acid
(+/-)-Pipecolate
alpha-Pipecolinic acid
(+/-)-Pipecolinate
2-Piperidinecarboxylate
Hexahydro-2-picolinate
Pipecolic acid free base
(+/-) pipecolic acid
Pipecolinic acid, 98%
DL-2-Piperidinecarboxylate
2-Piperidinylcarboxylic acid
2-piperidine carboxylic acid
2-piperidine-carboxylic acid
NCIOpen2_001582
SCHEMBL22016
(RS)-2-Piperidinecarboxylate
2-Piperidinecarboxylic acid #
PIPECOLIC ACID DL-FORM
dl-2-piperidinecarboxylic acid
CHEMBL308408
(+,-)-PIPECOLIC ACID
(+/-)-2-Piperidinecarboxylate
HXEACLLIILLPRG-UHFFFAOYSA-
rac piperidine-2-carboxylic acid
()-Piperidine-2-carboxylic acid
DTXCID70810951
(RS)-2-Piperidinecarboxylic acid
CS-B1313
HY-Y0669
NSC17125
NSC93089
AC-691
s6322
STL183326
AKOS000120345
AKOS016050399
(.+/-.)-2-Piperidinecarboxylic acid
2-Piperidinecarboxylic acid, (+/-)-
AB00554
AC-2835
FP34562
PS-5851
2-Piperidinecarboxylic acid, (A+/-)-
2-Piperidinecarboxylic acid, (.+/-.)-
SY002975
SY003075
SY003076
DB-038159
NS00074152
P0442
EN300-20680
Q7197255
F2191-0193
Z104479780
D(+)-Pipecolinic acid; (R)-(+)-2-Piperidinecarboxylic acid
InChI=1/C6H11NO2/c8-6(9)5-3-1-2-4-7-5/h5,7H,1-4H2,(H,8,9)
208-616-3
Solubility of Piperidine-2-carboxylic Acid
Piperidine-2-carboxylic acid, with the chemical formula C6H11NO2, exhibits interesting solubility characteristics that are notable for various applications in chemistry and biochemistry.
Solubility Characteristics:
As a result, piperidine-2-carboxylic acid is often utilized in an aqueous environment, enhancing its reactivity and interactions in systems where solubility is crucial. This characteristic makes it a valuable compound in both synthetic and medicinal chemistry.