90234-15-4

Basic information

• Product Name: Benzamide, 3-[[(dimethylamino)sulfonyl]amino]-N-2-pyridinyl-
• CAS NO: 90234-15-4
• Molecular Formula: C14H16N4O3S
• Molecular Weight: 320.372
• Mol File: 90234-15-4.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: Benzamide, 3-[[(dimethylamino)sulfonyl]amino]-N-2-pyridinyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzamide, 3-[[(dimethylamino)sulfonyl]amino]-N-2-pyridinyl-(90234-15-4)
• EPA Substance Registry System: Benzamide, 3-[[(dimethylamino)sulfonyl]amino]-N-2-pyridinyl-(90234-15-4)

Safety Data

• Hazardous Substances Data: 90234-15-4(Hazardous Substances Data)

Upstream product

• 121-90-4 m-nitrobenzoic acid chloride 
• 85367-01-7 3-nitro-N-(pyridin-2-yl)benzamide 
• 504-29-0 2-aminopyridine 
• 85367-02-8 3-amino-N-pyridin-2-yl-benzamide 
• 13360-57-1 dimethylamino sulfonyl chloride 

Relevant articles and documents

Synthesis and Antiviral Activity of Sulfonamidobenzophenone Oximes and Sulfonamidobenzamides

To find antiviral agents, various sulfonamidobenzophenone oximes (II) were synthesized from the appropriate m-sulfonamidobenzophenones by hydroxylamine reaction.The reaction products were generally obtained as syn/anti mixtures which were separable by fractional crystallization.The anti isomer had more potent antipoliovirus activity than the syn isomer.Various sulfonamidobenzamides (III) which were structurally related to II were synthesized by the reaction of amino-substituted benzamides with sulfuryl chloride or amines with (aminosulfonyl)benzoyl chloride.Antiviral activity was examined by the plaque-inhibition test.Compounds 5, 36, and 69 exhibited strong antipicornavirus activity.The structure-activity relationships are discussed.