21319-53-9 Usage
Uses
Used in Pharmaceutical Industry:
1-Benzylpiperidine-2-carboxylic acid is used as a therapeutic agent for its potential to treat various conditions, including inflammatory bowel disease, peptic ulcers, and traumatic brain injury. Its anti-inflammatory, wound healing, and tissue-protective properties make it a promising candidate for further research and development.
Used in Gastrointestinal Applications:
1-Benzylpiperidine-2-carboxylic acid is used as a healing agent for gastrointestinal tract issues, such as inflammatory bowel disease and peptic ulcers. Its ability to promote healing in the gastrointestinal tissue makes it a potential treatment option for these conditions.
Used in Musculoskeletal Applications:
1-Benzylpiperidine-2-carboxylic acid is used as a healing agent for muscle, tendon, and nerve tissue injuries. Its tissue-protective and wound healing properties make it a potential candidate for the treatment of musculoskeletal injuries and conditions.
Used in Neuroprotective Applications:
1-Benzylpiperidine-2-carboxylic acid is used as a neuroprotective agent for its potential to protect the brain from injury and promote healing in nerve tissue. This makes it a promising candidate for the treatment of traumatic brain injury and other neurological conditions.
Used in Hepatoprotective Applications:
1-Benzylpiperidine-2-carboxylic acid is used as a hepatoprotective agent for its potential to protect the liver from damage and promote healing in liver tissue. This makes it a potential candidate for the treatment of liver-related conditions.
Despite the promising potential of 1-Benzylpiperidine-2-carboxylic acid, further research is needed to fully understand its pharmacological mechanisms and potential uses in various applications.
Check Digit Verification of cas no
The CAS Registry Mumber 21319-53-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,3,1 and 9 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 21319-53:
(7*2)+(6*1)+(5*3)+(4*1)+(3*9)+(2*5)+(1*3)=79
79 % 10 = 9
So 21319-53-9 is a valid CAS Registry Number.
InChI:InChI=1/C13H17NO2/c15-13(16)12-8-4-5-9-14(12)10-11-6-2-1-3-7-11/h1-3,6-7,12H,4-5,8-10H2,(H,15,16)
21319-53-9Relevant academic research and scientific papers
Photoredox activation of carbon dioxide for amino acid synthesis in continuous flow
Seo, Hyowon,Katcher, Matthew H.,Jamison, Timothy F.
, p. 453 - 456 (2017/05/05)
Although carbon dioxide (CO 2) is highly abundant, its low reactivity has limited its use in chemical synthesis. In particular, methods for carbon-carbon bond formation generally rely on two-electron mechanisms for CO 2 activation and require highly activated reaction partners. Alternatively, radical pathways accessed via photoredox catalysis could provide new reactivity under milder conditions. Here we demonstrate the direct coupling of CO 2 and amines via the single-electron reduction of CO 2 for the photoredox-catalysed continuous flow synthesis of α-Amino acids. By leveraging the advantages of utilizing gases and photochemistry in flow, a commercially available organic photoredox catalyst effects the selective α-carboxylation of amines that bear various functional groups and heterocycles. The preliminary mechanistic studies support CO 2 activation and carbon-carbon bond formation via single-electron pathways, and we expect that this strategy will inspire new perspectives on using this feedstock chemical in organic synthesis.
The highly stereoselective formation of pipecolic acid N-oxide and related derivatives
O'Neil, Ian A.,Potter, Andrew J.
, p. 5731 - 5734 (2007/10/03)
N-Alkylated derivatives of pipecolic acid are shown to undergo highly stereoselective oxidation to give stable tertiary amine N-oxides. The ester derivatives show a high degree of stability compared to their proline analogues.
