105168-96-5

Basic information

• Product Name: (1,1-Dioxo-1H-1λ⁶-benzo[d]isothiazol-3-yl)-(2-ethoxy-4-nitro-phenyl)-amine
• CAS NO: 105168-96-5
• Molecular Weight: 347.351
• Mol File: 105168-96-5.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (1,1-Dioxo-1H-1λ⁶-benzo[d]isothiazol-3-yl)-(2-ethoxy-4-nitro-phenyl)-amine(CAS DataBase Reference)
• NIST Chemistry Reference: (1,1-Dioxo-1H-1λ⁶-benzo[d]isothiazol-3-yl)-(2-ethoxy-4-nitro-phenyl)-amine(105168-96-5)
• EPA Substance Registry System: (1,1-Dioxo-1H-1λ⁶-benzo[d]isothiazol-3-yl)-(2-ethoxy-4-nitro-phenyl)-amine(105168-96-5)

Safety Data

• Hazardous Substances Data: 105168-96-5(Hazardous Substances Data)

Upstream product

• 121-88-0 5-Nitro-2-aminophenol 
• 16383-89-4 5-nitro-2-amino-phenetole 
• 567-19-1 3-chloro-1,2-benzisothiazole 1,1-dioxide 

Downstream Products

• 105169-17-3 C₂₀H₂₁N₅O₇S 
• 105169-01-5 N¹-(1,1-Dioxo-1H-1λ⁶-benzo[d]isothiazol-3-yl)-2-ethoxy-benzene-1,4-diamine 

Relevant articles and documents

Quinone Imine Route to Benzimidazol-2-ylcarbamates. Part 3. Effect of Extension of Conjugation in the Quinone Imine.

5-Aminobenzimidazol-2-ylcarbamates (11) and (17), in which the amine is linked to position 3 of 1,2-benzisothiazole 1,1-dioxide have been synthesised in good yields from the guanidines (10) and (16) by oxidative cyclisation.The cyclisation is regiospecific.It is likely that quinone imines with extended conjugation are intermediates in this reaction.