22057-42-7

Basic information

• Product Name: 2-Nitro-4-methoxy-1-benzylmercapto-benzol
• Synonyms: 2-Nitro-4-methoxy-1-benzylmercapto-benzol
• CAS NO: 22057-42-7
• Molecular Weight: 275.328
• Mol File: 22057-42-7.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 2-Nitro-4-methoxy-1-benzylmercapto-benzol(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Nitro-4-methoxy-1-benzylmercapto-benzol(22057-42-7)
• EPA Substance Registry System: 2-Nitro-4-methoxy-1-benzylmercapto-benzol(22057-42-7)

Safety Data

• Hazardous Substances Data: 22057-42-7(Hazardous Substances Data)

Upstream product

• 100-44-7 benzyl chloride 
• 10298-80-3 2-chloro-5-methoxynitrobenzene 
• 100-53-8 phenylmethanethiol 

Downstream Products

• 72106-13-9 2-amino-4-methoxy-benzenesulfonamide 
• 686268-57-5 1-benzyl-4-hydroxy-3-(6-methoxy-1, 1-dioxido-4H-1,2,4-benzothiadiazin-3-yl)-1,8-naphthyridin-2(1H)-one 
• 81792-84-9 4-Methoxy-2-nitro-benzol-sulfonsaeure-⁽¹⁾-amid 

Relevant articles and documents

Inhibitors of HCV NS5B polymerase: Synthesis and structure-activity relationships of N-1-benzyl and N-1-[3-methylbutyl]-4-hydroxy-1,8-naphthyridon-3-yl benzothiadiazine analogs containing substituents on the aromatic ring

A series of non-nucleoside HCV NS5B polymerase inhibitors based on the N-1-benzyl or N-1-[3-methylbutyl]-4-hydroxy-1,8-naphthyridon-3-yl benzothiadiazine core substituted in the D-ring aromatic moiety have been prepared and evaluated. Aromatic substituents extending from position 7 of the D-ring exhibited excellent potency against both genotypes 1a and 1b.