117918-56-6 Usage
Description
1-(2-Furoyl)pyrrolidine-2-carboxylic acid is a chemical compound that belongs to the class of pyrrolidine carboxylic acids. It is an important precursor in the synthesis of pharmaceutical drugs and bioactive compounds, known for its potential applications in the field of medicinal chemistry, particularly in the development of new drug candidates. It is also used as a building block for the synthesis of various heterocyclic compounds, which have diverse biological activities. Additionally, 1-(2-Furoyl)pyrrolidine-2-carboxylic acid has been studied for its potential antioxidant and anti-inflammatory properties, making it a subject of interest for further pharmacological research.
Uses
Used in Pharmaceutical Industry:
1-(2-Furoyl)pyrrolidine-2-carboxylic acid is used as a precursor for the synthesis of pharmaceutical drugs and bioactive compounds, due to its potential applications in the development of new drug candidates.
Used in Medicinal Chemistry:
1-(2-Furoyl)pyrrolidine-2-carboxylic acid is used as a building block for the synthesis of various heterocyclic compounds, which have diverse biological activities, contributing to the advancement of medicinal chemistry.
Used in Antioxidant and Anti-Inflammatory Research:
1-(2-Furoyl)pyrrolidine-2-carboxylic acid is used as a subject of interest for further pharmacological research, due to its potential antioxidant and anti-inflammatory properties.
Check Digit Verification of cas no
The CAS Registry Mumber 117918-56-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,7,9,1 and 8 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 117918-56:
(8*1)+(7*1)+(6*7)+(5*9)+(4*1)+(3*8)+(2*5)+(1*6)=146
146 % 10 = 6
So 117918-56-6 is a valid CAS Registry Number.
InChI:InChI=1/C10H11NO4/c12-9(8-4-2-6-15-8)11-5-1-3-7(11)10(13)14/h2,4,6-7H,1,3,5H2,(H,13,14)/p-1/t7-/m1/s1
117918-56-6Relevant articles and documents
Rapid photoassisted access to N,O,S-polyheterocycles with benzoazocine and hydroquinoline cores: Intramolecular cycloadditions of photogenerated azaxylylenes
Mukhina, Olga A.,Bhuvan Kumar,Arisco, Teresa M.,Valiulin, Roman A.,Metzel, Greg A.,Kutateladze, Andrei G.
supporting information; experimental part, p. 9423 - 9428 (2011/11/06)
Ring the changes: A new photoassisted approach to give conformationally constrained N,O,S-polyheterocyclic scaffolds of unprecedented topologies was achieved by intramolecular [4+4] and [4+2] cycloadditions of photogenerated o-azaxylylenes (23 examples; see scheme). The precursors can be readily assembled by simple and high-yielding reactions, thus making this a powerful synthetic method amenable to high-throughput diversity-oriented synthesis.