283587-22-4 Usage
Class
Thiadiazolidinones
Structure
Contains a benzene ring with a methoxy group attached to the fourth position and a thiadiazolidin-3-one ring system. Also has two methyl groups attached to the carbon atoms adjacent to the dioxo group on the thiadiazolidin-3-one ring.
Potential applications
Pharmaceutical and medicinal chemistry
Further research
Synthesis, properties, and possible uses in various fields
Check Digit Verification of cas no
The CAS Registry Mumber 283587-22-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,8,3,5,8 and 7 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 283587-22:
(8*2)+(7*8)+(6*3)+(5*5)+(4*8)+(3*7)+(2*2)+(1*2)=174
174 % 10 = 4
So 283587-22-4 is a valid CAS Registry Number.
InChI:InChI=1/C12H16N2O4S/c1-12(2)11(15)13-19(16,17)14(12)8-9-4-6-10(18-3)7-5-9/h4-7H,8H2,1-3H3,(H,13,15)
283587-22-4Relevant articles and documents
Solid phase synthesis of sulfahydantoins
Albericio, Fernando,Garcia, Javier,Michelotti, Enrique L.,Nicolás, Ernesto,Tice, Colin M.
, p. 3161 - 3163 (2000)
A five step solid phase synthesis of 2-unsubstituted 1,2,5- thiadiazolidin-3-one 1,1-dioxides (sulfahydantoins) from N(α)-FMOC-amino acids and aromatic aldehydes is described. The key step is the base mediated cyclitive cleavage of a resin bound N(α)-(aminosulfonyl)-N(α)-benzyl-amino acid to afford the desired product. This synthesis allows the preparation of a diverse library of compounds based on this heterocycle. (C) 2000 Elsevier Science Ltd.
