117918-56-6 Usage
General 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. 1-(2-FUROYL)PYRROLIDINE-2-CARBOXYLIC ACID is 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.
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.
