14773-85-4

Basic information

• Product Name: Isocyanatosulfuric acid, phenyl ester
• CAS NO: 14773-85-4
• Molecular Formula: C7H5NO4S
• Molecular Weight: 199.187
• Mol File: 14773-85-4.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Isocyanatosulfuric acid, phenyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Isocyanatosulfuric acid, phenyl ester(14773-85-4)
• EPA Substance Registry System: Isocyanatosulfuric acid, phenyl ester(14773-85-4)

Safety Data

• Hazardous Substances Data: 14773-85-4(Hazardous Substances Data)

Upstream product

• 1189-71-5 isocyanate de chlorosulfonyle 
• 108-95-2 phenol 

Downstream Products

• 112222-22-7 2,6-Di-tert-butylcyclohexanthiocarbonsaeure-O-phenylester 
• 112222-21-6 5-(2,6-Di-tert-butylcyclohexyl)-N-(phenoxysulfonyl)-3H-1,2,4-dithiazol-3-imin 
• 120343-28-4 N-(adamantyl-1) sulfamate de phenyle 
• 120343-34-2 N-(phenoxysulfonyl) carbamate d'adamantyle-2 
• 72119-38-1 N,N'-bisphenoxysulfonyl-piperazine 
• 233756-84-8 4-hydroxymethyl-3-phenoxysulfonyl-1,3-oxazolidin-2-one 
• 233756-80-4 glycidyl phenoxysulfonylcarbamate 

Relevant articles and documents

NOVEL SULFONAMIDE DERIVATIVE

A compound of the formula (1): wherein m, n and p is independently an integer of 0 to 4 with the proviso that 3 a?| m + n a?| 8; X is the formula: NR4, etc.; R1, R3 and R4 are a substituted or unsubstituted aryl group, etc.; R2 is a hydrogen atom, etc.; a, b, c, d, e and f are a hydrogen atom or a substituted or unsubstituted alkyl group, etc.; Y is the formula: -SO2-, etc.; and Z is an oxygen atom, etc.; or a prodrug thereof or a pharmaceutically acceptable salt of the same has an activity of potentiating an expression of a low density lipoprotein receptor and thus is useful as an agent for treating hyperlipidemia or arteriosclerosis.

SYNTHESES A L'AIDE D'HETEROCUMULENES. 3. NOUVELLES OXAZOLIDINONES-2 ET IMIDAZOLIDINONES-2 A PARTIR DE L'ISOCYANATE DE PHENOXYSULFONYLE.

We report here, the first use in heterocyclic synthesis of the phenoxysulfonyl isocyanate that reacts with ω-halogeno-alcohols and β-halogeno-ethylamines to give a new family of 2-oxazolidinones and 2-imidazolidinones.