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6339-87-3

6339-87-3 Structure

6339-87-3 Structure
IdentificationMore
[Name]

Thiophene-2-sulfonamide
[CAS]

6339-87-3
[Synonyms]

BUTTPARK 44\07-11
THIOPHENE-2-SULFONAMIDE
THIOPHENE-ALPHA-SULFONAMIDE
THIOPHENE-A-SULFONAMIDE
2-thiophenesulfonamide
2-Thienylsulfonamide
THIOPHENE-α-SULFONAMIDE
2-Thiophenesulfonamide(6CI,7CI,8CI,9CI)
THIOPHENE-2-SULFONIC ACID AMIDE
Thiophene-2-sulphonamide
[Molecular Formula]

C4H5NO2S2
[MDL Number]

MFCD00185853
[Molecular Weight]

163.22
[MOL File]

6339-87-3.mol
Chemical PropertiesBack Directory
[Melting point ]

137-141 °C
[Boiling point ]

338.1±34.0 °C(Predicted)
[density ]

1.513±0.06 g/cm3(Predicted)
[storage temp. ]

Keep in dark place,Sealed in dry,Room Temperature
[solubility ]

soluble in Methanol
[form ]

powder to crystal
[pka]

9.94±0.60(Predicted)
[color ]

White to Light yellow to Light orange
[InChI]

1S/C4H5NO2S2/c5-9(6,7)4-2-1-3-8-4/h1-3H,(H2,5,6,7)
[InChIKey]

KTFDYVNEGTXQCV-UHFFFAOYSA-N
[SMILES]

NS(=O)(=O)c1cccs1
[CAS DataBase Reference]

6339-87-3(CAS DataBase Reference)
Safety DataBack Directory
[Hazard Codes ]

Xi
[Risk Statements ]

36/37/38
[Safety Statements ]

26
[WGK Germany ]

3
[RTECS ]

XN0294000
[HS Code ]

29350090
[Storage Class]

11 - Combustible Solids
[Hazard Classifications]

Eye Irrit. 2
Skin Irrit. 2
STOT SE 3
Hazard InformationBack Directory
[Definition]

ChEBI: 2-Thiophenesulfonamide is a member of thiophenes.
[Synthesis Reference(s)]

Tetrahedron Letters, 35, p. 7201, 1994 DOI: 10.1016/0040-4039(94)85360-6
[Synthesis]

2-Thiophenesulfonyl chloride

16629-19-9

Thiophene-2-sulfonamide

6339-87-3

General procedure for the synthesis of 2-thiophenesulfonamide from 2-thiophenesulfonyl chloride: Example: preparation of 2-thiophenesulfonamide 2-Thiophenesulfonyl chloride (0.5 g, 2.74 mmol) was added to 25% ammonium hydroxide solution (5 mL, 33.45 mmol), refluxed and stirred at 50°C for 15 hours. Upon completion of the reaction, the reaction mixture was filtered while hot and the residue was washed with boiling aqueous 25% ammonium hydroxide solution. Subsequently, the ammonium hydroxide solution was removed by vacuum distillation until there was no ammonia odor. Eventually, 2-thiophenesulfonamide was recrystallized from water to give a white solid (0.328 g, 77% yield). Product Characterization: Melting point: 145-146°C; IR spectrum (KBr, cm?1): 3290 (N-H stretching vibration), 3224 (N-H stretching vibration); NMR hydrogen spectrum (400 MHz, DMSO-d6, δ): 7.15 (1H, dd, J = 5.0, 3.7 Hz, C(4)H), 7.55 (1H, dd, J = 3.7, 1.4 Hz, C(3)H), 7.66 (2H, s, NH2), 7.85 (1H, dd, J = 5.0, 1.4 Hz, C(5)H); NMR carbon spectrum (100 MHz, DMSO-d6, δ): 127.3, 130.0, 131.1, 145.7; Mass spectrum (ESI?): m/z 162 ([M-H]? , 100%); High-resolution mass spectrum (ESI?): C4H4NO2S2 ([M-H]?) Calculated value 161.9689, measured value 161.9695.

[References]

[1] Journal of the American Chemical Society, 2010, vol. 132, # 10, p. 3238 - 3239
[2] Patent: WO2011/55142, 2011, A2. Location in patent: Page/Page column 47
[3] Phosphorus and Sulfur and the Related Elements, 1981, vol. 10, p. 111 - 120
[4] Phosphorus and Sulfur and the Related Elements, 1980, vol. 8, p. 197 - 200
[5] Justus Liebigs Annalen der Chemie, 1933, vol. 501, p. 174,182
Spectrum DetailBack Directory
[Spectrum Detail]

Thiophene-2-sulfonamide(6339-87-3)1HNMR
Well-known Reagent Company Product InformationBack Directory
[Sigma Aldrich]

6339-87-3(sigmaaldrich)
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