ChemicalBook > CAS DataBase List > N-(4-ACETYL-PHENYL)-METHANESULFON-AMIDE

N-(4-ACETYL-PHENYL)-METHANESULFON-AMIDE

Product Name
N-(4-ACETYL-PHENYL)-METHANESULFON-AMIDE
CAS No.
5317-89-5
Chemical Name
N-(4-ACETYL-PHENYL)-METHANESULFON-AMIDE
Synonyms
AURORA 2940;N-(4-Acetylphenyl);4'-ACETYLMETHANESULFONANILIDE;4'-Acetylmethanesulfonanilide;N-(4-ethanoylphenyl)methanesulfonamide;Methanesulfonamide, N-(4-acetylphenyl)-;N-(4-ACETYL-PHENYL)-METHANESULFON-AMIDE
CBNumber
CB4461135
Molecular Formula
C9H11NO3S
Formula Weight
213.25
MOL File
5317-89-5.mol
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N-(4-ACETYL-PHENYL)-METHANESULFON-AMIDE Property

Melting point:
150-152 °C
Boiling point:
369.4±44.0 °C(Predicted)
Density 
1.320±0.06 g/cm3(Predicted)
storage temp. 
Sealed in dry,Room Temperature
pka
7.16±0.10(Predicted)
Appearance
White to light yellow Solid
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Safety

Hazard Codes 
Xi
HazardClass 
IRRITANT
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H302Harmful if swallowed

H315Causes skin irritation

H319Causes serious eye irritation

H335May cause respiratory irritation

Precautionary statements

P261Avoid breathing dust/fume/gas/mist/vapours/spray.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

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N-Bromosuccinimide Price

TRC
Product number
N497065
Product name
N-(4-Acetylphenyl)methanesulfonamide
Packaging
100mg
Price
$60
Updated
2021/12/16
TRC
Product number
N497065
Product name
N-(4-Acetylphenyl)methanesulfonamide
Packaging
500mg
Price
$110
Updated
2021/12/16
Biosynth Carbosynth
Product number
FA114576
Product name
N-(4-Acetylphenyl)methanesulfonamide
Packaging
250mg
Price
$57.5
Updated
2021/12/16
Biosynth Carbosynth
Product number
FA114576
Product name
N-(4-Acetylphenyl)methanesulfonamide
Packaging
500mg
Price
$100
Updated
2021/12/16
Matrix Scientific
Product number
030126
Product name
N-(4-Acetylphenyl)methanesulfonamide
Packaging
500mg
Price
$86
Updated
2021/12/16
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N-(4-ACETYL-PHENYL)-METHANESULFON-AMIDE Chemical Properties,Usage,Production

Synthesis

99-92-3

124-63-0

5317-89-5

Cooled 4-aminoacetophenone (10 mmol) was dissolved in pyridine (10 mL) at 0 °C and methanesulfonyl chloride (15 mmol) was added slowly. The reaction mixture was stirred at room temperature for 2 hours. After completion of the reaction, the reaction mixture was diluted with H2O and extracted with ethyl acetate (EtOAc) several times. The organic layers were combined, washed sequentially with H2O and saturated brine and dried over anhydrous magnesium sulfate (MgSO4). After filtration, the filtrate was concentrated under reduced pressure. The residue was purified by rapid column chromatography on silica gel, the eluent being a mixed solvent of ethyl acetate:hexane to afford N-(4-acetylphenyl)methanesulfonamide (Compound 13-5, LJO-298). The yield was 95% and the melting point was 161 °C. 1H NMR (CDCl3) δ: 7.97 (dd, 2H, J = 2.0, 6.8 Hz), 7.26 (dd, 2H, J = 2.0, 6.8 Hz), 6.87 (bs, 1H), 3.10 (s, 3H), 2.59 (s, 3H).

References

[1] Journal of Enzyme Inhibition and Medicinal Chemistry, 2014, vol. 29, # 6, p. 846 - 867
[2] Organic Process Research and Development, 1998, vol. 2, # 2, p. 71 - 77
[3] Bioorganic and Medicinal Chemistry, 2007, vol. 15, # 18, p. 6043 - 6053
[4] Bioorganic and Medicinal Chemistry Letters, 2014, vol. 24, # 12, p. 2685 - 2688
[5] Patent: WO2005/3084, 2005, A1. Location in patent: Page 79

N-(4-ACETYL-PHENYL)-METHANESULFON-AMIDE Preparation Products And Raw materials

Raw materials

Preparation Products

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