197959-76-5

Basic information

• Product Name: 3-(5-chloro-2-methoxyphenylsulfonyloxy)-5-methylphenol
• Synonyms: 3-(5-chloro-2-methoxyphenylsulfonyloxy)-5-methylphenol
• CAS NO: 197959-76-5
• Molecular Weight: 328.773
• Mol File: 197959-76-5.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 3-(5-chloro-2-methoxyphenylsulfonyloxy)-5-methylphenol(CAS DataBase Reference)
• NIST Chemistry Reference: 3-(5-chloro-2-methoxyphenylsulfonyloxy)-5-methylphenol(197959-76-5)
• EPA Substance Registry System: 3-(5-chloro-2-methoxyphenylsulfonyloxy)-5-methylphenol(197959-76-5)

Safety Data

• Hazardous Substances Data: 197959-76-5(Hazardous Substances Data)

Upstream product

• 22952-32-5 5-chloro-2-methoxybenzenesulfonyl chloride 
• 144-55-8 sodium hydrogencarbonate 
• 6153-39-5 5-Methylresorcinol monohydrate 
• 504-15-4 orcinol 

Downstream Products

• 197960-30-8 3-(2-Methoxyphenylsulfonyloxy)-5-methylphenoxyacetaldehyde 
• 197960-77-3 2-[3-(2-Methoxyphenylsulfonyloxy)-5-methylphenoxy]ethanol 
• 197959-79-8 3-[3-(2-methoxyphenylsulfonyloxy)-5-methylphenoxy]propionaldehyde 
• 197960-21-7 4-[3-(2-Methoxyphenylsulfonyloxy)-5-methylphenoxy]butyraldehyde 
• 197959-78-7 3-[3-(2-methoxyphenylsulfonyloxy)-5-methylphenoxy]propanol 
• 197960-20-6 4-[3-(2-methoxyphenylsulfonyloxy)-5-methylphenoxy]butanol 
• 197959-77-6 3-(2-methoxyphenylsulfonyloxy)-5-methylphenol 
• 197960-07-9 3-[3-(5-chloro-2-methoxyphenylsulfonyloxy)-5-methylphenoxy]-propanol 

Relevant articles and documents

AMIDINOHYDRAZONES AS PROTEASE INHIBITORS

Amidino and benzamidino compounds, including compounds of the formula: I wherein R1-R4, R6-R9, Y, Z, n and m are set forth in the specification, as well as hydrates, solvates or pharmaceutically acceptable salts thereof, that inhibit proteolytic enzymes such as thrombin are described. Also described are methods for preparing the compounds of Formula I.

Amidinohydrazones as guanidine bioisosteres: Application to a new class of potent, selective and orally bioavailable, non-amide-based small-molecule thrombin inhibitors

We describe a new class of potent, non-amide-based small molecule thrombin inhibitors in which an amidinohydrazone is used as a guanidine bioisostere on a non-peptide scaffold. Compound 4 exhibits nM inhibition of thrombin, is selective for thrombin, and