ChemicalBook--->CAS DataBase List--->73901-01-6

73901-01-6

73901-01-6 Structure

73901-01-6 Structure
IdentificationBack Directory
[Name]

2,4-dinitrobenzenesulfonamide
[CAS]

73901-01-6
[Synonyms]

2,4-dinitrobenzenesulfonamide
Benzenesulfonamide, 2,4-dinitro-
[Molecular Formula]

C6H5N3O6S
[MDL Number]

MFCD09733471
[MOL File]

73901-01-6.mol
[Molecular Weight]

247.19
Chemical PropertiesBack Directory
[storage temp. ]

Sealed in dry,Room Temperature
[Appearance]

White to yellow Solid
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H335-H319-H315
[Precautionary statements ]

P264-P280-P302+P352-P321-P332+P313-P362-P264-P280-P305+P351+P338-P337+P313P
Hazard InformationBack Directory
[Uses]

2,4-Dinitrobenzenesulfonamide can be used as a drug for hypertension and type 2 diabetes mellitus.
[Synthesis]

4-NITROBENZENESULFONYL FLUORIDE

349-96-2

2,4-dinitrobenzenesulfonamide

73901-01-6

GENERAL METHOD: p-Nitrobenzene methanesulfonyl fluoride (0.5 mmol) was dissolved in acetonitrile (1 mL), and 1,8-diazabicycloundec-7-ene (DBU, 22 μL, 0.15 mmol, 0.3 eq.) and trimethylsilyl azide (TMSN3, 50 μL, 0.375 mmol, 0.75 eq.) were added in sequence. The reaction mixture was stirred at room temperature for 15 min before trimethylsilyl azide (TMSN3, 50 μL, 0.375 mmol, 0.75 equiv) was added again. Stirring was continued for 45 min and after completion of the reaction, the reaction was filtered through a short column of silica gel, eluting with ethyl acetate (50 mL). The filtrate was concentrated under reduced pressure to remove the volatile solvent to afford the target product 2,4-dinitrobenzenesulfonamide.

[References]

[1] Synlett, 2016, vol. 27, # 12, p. 1840 - 1843
Spectrum DetailBack Directory
[Spectrum Detail]

2,4-dinitrobenzenesulfonamide(73901-01-6)1HNMR
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