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.