N-Isopropylbenzenesulfonamide
- Product Name
- N-Isopropylbenzenesulfonamide
- CAS No.
- 5339-69-5
- Chemical Name
- N-Isopropylbenzenesulfonamide
- Synonyms
- N-Isopropylbenzenesulfonamide;N-propan-2-ylbenzenesulfonamide;N-(1-Methylethyl)benzenesulfonamide;Benzenesulfonamide, N-(1-methylethyl)-
- CBNumber
- CB02415453
- Molecular Formula
- C9H13NO2S
- Formula Weight
- 199.27
- MOL File
- 5339-69-5.mol
N-Isopropylbenzenesulfonamide Property
- storage temp.
- Sealed in dry,Room Temperature
- solubility
- Chloroform (Slightly), Methanol (Slightly)
- form
- Oil
- color
- Colourless
Safety
- HS Code
- 2935909099
Hazard and Precautionary Statements (GHS)
- Symbol(GHS)
-
- Signal word
- Warning
- Hazard statements
-
H302Harmful if swallowed
- Precautionary statements
-
P264Wash hands thoroughly after handling.
P264Wash skin thouroughly after handling.
P270Do not eat, drink or smoke when using this product.
P501Dispose of contents/container to..…
N-Bromosuccinimide Price
- Product number
- I874673
- Product name
- N-Isopropylbenzenesulfonamide
- Packaging
- 50mg
- Price
- $45
- Updated
- 2021/12/16
- Product number
- I874673
- Product name
- N-Isopropylbenzenesulfonamide
- Packaging
- 100mg
- Price
- $60
- Updated
- 2021/12/16
- Product number
- I874673
- Product name
- N-Isopropylbenzenesulfonamide
- Packaging
- 500mg
- Price
- $200
- Updated
- 2021/12/16
- Product number
- OR958001
- Product name
- N-Isopropylbenzenesulfonamide
- Purity
- 95%
- Packaging
- 250mg
- Price
- $211
- Updated
- 2021/12/16
- Product number
- 7593AB
- Product name
- N-Isopropylbenzenesulfonamide
- Packaging
- 1g
- Price
- $253
- Updated
- 2021/12/16
N-Isopropylbenzenesulfonamide Chemical Properties,Usage,Production
Uses
N-Isopropylbenzenesulfonamide can be used to treat hypertension.
Synthesis
98-10-2
67-63-0
5339-69-5
GENERAL METHOD: Benzenesulfonamide (2 mmol) was dissolved with isopropanol (10 mmol) in 1,4-dioxane (3 mL), followed by the addition of trifluoromethanesulfonic anhydride (Tf2O, 2 mmol). The reaction mixture was sealed and the reaction was stirred at 120 °C until thin layer chromatography (TLC) monitoring showed that the reaction was complete. After completion of the reaction, the reaction was quenched with saturated aqueous sodium bicarbonate (NaHCO3). The reaction mixture was extracted three times with ethyl acetate (EtOAc) and the organic phases were combined and dried with anhydrous sodium sulfate (Na2SO4). After concentration under reduced pressure to remove the solvent, the residue was purified by fast column chromatography using petroleum ether (PE) and ethyl acetate (EtOAc) (3:1, v/v/v) as eluents to give pure N-isopropylbenzenesulfonamide (IBSA).
References
[1] Bulletin of the Chemical Society of Japan, 2015, vol. 88, # 4, p. 610 - 612
N-Isopropylbenzenesulfonamide Preparation Products And Raw materials
Raw materials
Preparation Products
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