21319-53-9 Usage
General Description
1-Benzylpiperidine-2-carboxylic acid, also known as BPC-157, is a synthetic peptide compound derived from a small protein found in the stomach and has been shown to have potential therapeutic effects. It is a peptide chain consisting of 15 amino acids and has been researched for its anti-inflammatory, wound healing, and tissue-protective properties. BPC-157 has been studied for its ability to promote healing in various tissues, including the gastrointestinal tract, muscle, tendon, and nerve tissue. It is also believed to have protective effects on the liver and brain, making it a potential candidate for the treatment of various conditions such as inflammatory bowel disease, peptic ulcers, and traumatic brain injury. Despite its promising potential, further research is needed to fully understand the pharmacological mechanisms and potential uses of BPC-157.
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 articles and documents
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.
