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Energy Chemical |
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| | 2-(Phenylsulfonyl)aniline Basic information |
| | 2-(Phenylsulfonyl)aniline Chemical Properties |
| Melting point | 120-122 °C(lit.) | | Boiling point | 439.6±28.0 °C(Predicted) | | density | 1.295±0.06 g/cm3(Predicted) | | pka | -1.06±0.10(Predicted) | | form | solid | | color | Pale yellow | | InChI | 1S/C12H11NO2S/c13-11-8-4-5-9-12(11)16(14,15)10-6-2-1-3-7-10/h1-9H,13H2 | | InChIKey | JBCUKQQIWSWEOK-UHFFFAOYSA-N | | SMILES | Nc1ccccc1S(=O)(=O)c2ccccc2 | | CAS DataBase Reference | 4273-98-7(CAS DataBase Reference) | | EPA Substance Registry System | o-Aminodiphenyl sulfone (4273-98-7) |
| Hazard Codes | Xn,Xi | | Risk Statements | 36/37/38-22 | | Safety Statements | 36/37/39-26 | | WGK Germany | 3 | | Hazard Note | Irritant | | TSCA | TSCA listed | | HS Code | 29214200 | | Storage Class | 11 - Combustible Solids |
| | 2-(Phenylsulfonyl)aniline Usage And Synthesis |
| Chemical Properties | off-white to beige powder | | Uses | 2-(Phenylsulfonyl)aniline may be used in chemical synthesis. | | Preparation | Preparationofthechromophore : Will 1-(2-Nitrophenylsulfonyl)benzenerestored. | | Synthesis | General procedure for the synthesis of 2-aminodiphenyl sulfone from 2-nitrodiphenyl sulfone: 5.22 g (0.09315 mol) of iron powder was added in batches to a 60 mL suspension of acetic acid containing 4.9 g (0.01863 mol) of 2-nitrodiphenyl sulfone. The reaction mixture was stirred at 70°C for 3 hours, followed by cooling and filtration to remove inorganic impurities. To the filtrate was added 100 mL of water, and the precipitate precipitated was filtered, washed with water, and dried under vacuum to give 4 g (92% yield) of 2-(phenylsulfonyl)aniline (10f). The product was analyzed by mass spectrometry (LS MC m/z 234 (M + 1)) and 1H NMR (DMSO-d6, 400 MHz) δ 7.91 (d, J = 8Hz, 2H), 7.67 (t, J = 9.6Hz, 2H), 7.58 (t, J = 7.6Hz, 2H), 7.29 (t, J = 7.2Hz, 1H), 6.77 (d, J = 8.4 Hz, 1H), 6.67 (t, J = 7.6 Hz, 1H), 6.12 (s, 2H) confirmed. | | Properties and Applications | the fastness properties in cotton:
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Couplingcomponents
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Fast light
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Soda boiling
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Oxygen bleaching
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Ironing
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Chlorine bleaching
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|
ISO
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AATCC
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ISO
|
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1/3N
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2N
|
2N
|
|
8
|
5
|
|
6-7
|
4
|
2
|
3-4
|
4-5
|
|
11
|
5
|
|
5-6
|
|
1-2
|
|
4-5
|
|
12
|
5
|
|
6
|
2-3
|
1-2
|
4-5
|
4
|
|
20
|
5
|
|
6-7
|
3-4
|
1
|
3-4
|
4-5
|
|
24
|
5
|
|
6-7
|
4
|
2
|
3-4
|
4-5
|
| | References | [1] Bioorganic and Medicinal Chemistry, 2013, vol. 21, # 15, p. 4614 - 4627
[2] Helvetica Chimica Acta, 1980, vol. 63, # 6, p. 1412 - 1419
[3] Journal of the American Chemical Society, 1950, vol. 72, p. 965,969
[4] Journal of the Chemical Society, 1938, p. 899,902
[5] Chemische Berichte, 1901, vol. 34, p. 1155 |
| | 2-(Phenylsulfonyl)aniline Preparation Products And Raw materials |
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