66892-63-5

Basic information

• Product Name: 6''-FLUORO-2'',3''-DIHYDRO-2H,5H-SPIRO[IMIDAZOLIDINE-4,4''-THIOCHROMENE]-2,5-DIONE 1'',1''-DIOXIDE
• Synonyms: 6-FLUOROSPIRO[IMIDAZOLIDINE-4,4-THIOCHROMAN]-2,5-DIONE 1,1-DIOXIDE
• CAS NO: 66892-63-5
• Molecular Formula: C11H9FN2O4S
• Molecular Weight: 284.266
• Mol File: 66892-63-5.mol
• Article Data: 2

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 6''-FLUORO-2'',3''-DIHYDRO-2H,5H-SPIRO[IMIDAZOLIDINE-4,4''-THIOCHROMENE]-2,5-DIONE 1'',1''-DIOXIDE(CAS DataBase Reference)
• NIST Chemistry Reference: 6''-FLUORO-2'',3''-DIHYDRO-2H,5H-SPIRO[IMIDAZOLIDINE-4,4''-THIOCHROMENE]-2,5-DIONE 1'',1''-DIOXIDE(66892-63-5)
• EPA Substance Registry System: 6''-FLUORO-2'',3''-DIHYDRO-2H,5H-SPIRO[IMIDAZOLIDINE-4,4''-THIOCHROMENE]-2,5-DIONE 1'',1''-DIOXIDE(66892-63-5)

Safety Data

• Hazardous Substances Data: 66892-63-5(Hazardous Substances Data)

Upstream product

• 66892-47-5 6'-fluoro-spiro[imidazolidine-4,4'-thiochroman]-2,5-dione 
• 21243-18-5 6-fluoro-3,4-dihydro-2H-1-benzothiopyran-4-one 

Relevant articles and documents

Spiro hydantoin aldose reductase inhibitors

Sorbitol formation from glucose, catalyzed by the enzyme aldose reductase, is believed to play a role in the development of certain chronic complications of diabetes mellitus. Spiro hydantoin derived from five- and six-membered ketones fused to an aromatic ring or ring system inhibit aldose reductase isolated from calf lens. In vivo these compounds are potent inhibitors of sorbitol formation in sciatic nerves of streptozotocinized rats. Optimum in vivo activity is reached in spiro hydantoins derived from 6-halogenated 2,3-dihydro-4H-1-benzopyran-4-ones (4-chromanones). In 2,4-dihydro-6-fluorospirol[4H-1-benzopyran-4,4'-imidazolidine]-2',5'- ione, the activity resides exclusively in the 4S isomer, compound 115 (CP-45,634, USAN: sorbinil). This compound is currently being used to test, in humans, the value of aldose reductase inhibitors in the therapy of diabetic complications.