5652-37-9 Usage
Uses
Used in Pharmaceutical Industry:
3-(2-Furoylamino)propanoic acid is used as a potential therapeutic agent for the treatment of cardiovascular diseases. Its antithrombotic and antiplatelet properties make it a promising candidate for managing conditions related to blood clotting and platelet aggregation.
3-(2-Furoylamino)propanoic acid is used as an inhibitor of thromboxane A2 activity, which helps prevent the adhesion of blood platelets to injured blood vessel walls. This action is crucial in reducing the risk of thrombosis and associated complications in cardiovascular health.
In the Drug Development Sector:
3-(2-Furoylamino)propanoic acid is utilized in the research and development of new drugs targeting cardiovascular conditions. Its unique chemical structure and biological activity provide a foundation for designing innovative pharmaceuticals that could offer improved treatment options for patients suffering from heart diseases and related disorders.
Check Digit Verification of cas no
The CAS Registry Mumber 5652-37-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,6,5 and 2 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 5652-37:
(6*5)+(5*6)+(4*5)+(3*2)+(2*3)+(1*7)=99
99 % 10 = 9
So 5652-37-9 is a valid CAS Registry Number.
InChI:InChI=1/C8H9NO4/c10-7(11)3-4-9-8(12)6-2-1-5-13-6/h1-2,5H,3-4H2,(H,9,12)(H,10,11)
5652-37-9Relevant academic research and scientific papers
Liang, Yuan-Wei,Liao, Xiao-Jian,Wang, Chang-Jun,Guo, Jin-Zhi,Li, Shuo,Xu, Shi-Hai
, p. 736 - 737 (2012)
The first total synthesis of the furanolactam fuscain is reported. The key step in the synthesis was the formation of seven-membered lactam by acylation of a furan ring using the mild Lewis acid CuSO4·5H2O.
Visible light-mediated synthesis of (Spiro)anellated furans
Kachkovskyi, Georgiy,Faderl, Christian,Reiser, Oliver
supporting information, p. 2240 - 2248 (2013/10/01)
Visible light-mediated decarboxylation using N-acyloxyphthalimides as the source for carbon-centered radicals was applied for the synthesis of spirobutenolides. The utility of this approach is demonstrated with the formal synthesis of (S)-(+)-lycoperdic acid. Alternatively, 2,3-anellated furans can be obtained in a one-pot procedure via photocyclization following a regioselective semipinacol rearrangement.
