165668-35-9

Basic information

• Product Name: 4-methoxy-N-(7-indazolyl)benzenesulfonamide
• Synonyms: 4-methoxy-N-(7-indazolyl)benzenesulfonamide
• CAS NO: 165668-35-9
• Molecular Weight: 303.342
• Mol File: 165668-35-9.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 4-methoxy-N-(7-indazolyl)benzenesulfonamide(CAS DataBase Reference)
• NIST Chemistry Reference: 4-methoxy-N-(7-indazolyl)benzenesulfonamide(165668-35-9)
• EPA Substance Registry System: 4-methoxy-N-(7-indazolyl)benzenesulfonamide(165668-35-9)

Safety Data

• Hazardous Substances Data: 165668-35-9(Hazardous Substances Data)

Upstream product

• 64-17-5 ethanol 
• 98-68-0 4-methoxy-phenyl-sulphonyl chloride 
• 2942-42-9 7-Nitroindazole 
• 21443-96-9 1H-indazol-7-amine 

Downstream Products

• 865604-02-0 4-methoxy-N-methyl-N-(3-bromo-4-(4-methoxyphenyl)-1-methyl-7-indazolyl)benzenesulfonamide 
• 865603-95-8 N-(3,4-diiodo-1H-indazol-7-yl)-4-methoxy-N-methyl-benzenesulfonamide 
• 865603-96-9 4-methoxy-N-methyl-N-(3,4-diiodo-1-methyl-7-indazolyl)benzenesulfonamide 
• 865604-00-8 N-(3-bromo-4-iodo-1H-indazol-7-yl)-4-methoxy-N-methyl-benzenesulfonamide 
• 865604-01-9 N-(3-bromo-4-iodo-1-methyl-1H-indazol-7-yl)-4-methoxy-N-methyl-benzenesulfonamide 
• 865603-94-7 N-(4-iodo-1H-indazol-7-yl)-4-methoxy-N-methyl-benzenesulfonamide 
• 865603-97-0 4-methoxy-N-methyl-N-(7-indazolyl)benzenesulfonamide 
• 865603-87-8 4-methoxy-N-(4-iodo-7-indazolyl)benzenesulfonamide 

Relevant articles and documents

Synthesis and biological evaluation of N-(7-indazolyl)benzenesulfonamide derivatives as potent cell cycle inhibitors

We herein describe a new synthesis of N-(7-indazolyl)benzenesulfonamide derivatives. These compounds were evaluated for their antiproliferative activities toward L1210 murine leukemia cells. One of them, 4-methoxy-N-(3- chloro-7-indazolyl)benzenesulfonamide, was identified as the most potent with an IC50 of 0.44 μM.

New and efficient synthesis of bi- and trisubstituted indazoles

In this paper, the synthesis of bi- and trisubstituted indazoles was described. 4-Alkoxy-7-aminoprotected-indazole or 7-aminoprotected-indazole derivatives were prepared selectively using SnCl2 in alcohol or SnCl2 in ethyl acetate, r