4-(2-Aminoethyl)benzenesulfonamide
| Product Name |
4-(2-Aminoethyl)benzenesulfonamide
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| Product Code |
A00008357
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| Chemical name |
4-(2-Aminoethyl)benzenesulfonamide
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| Synonyms |
p-(2-Aminoethyl)benzenesulfonamide; 2-(4-Sulfamoylphenyl)ethylamine; 2-[4-(Aminosulfonyl)phenyl]ethylamine; 4-(2-Aminoethyl)benzensulfonamide; 4-(Aminosulfonyl)phenethylamine; 4-Sulfamoylphenethylamine; p-(β-Aminoethyl)benzenesulfonamide; p-Aminoethyl-benzenesulfonamide
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| Impurity |
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| CAS Number |
35303-76-5
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| Alternate CAS # |
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| Molecular form |
C₈H₁₂N₂O₂S
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| Appearance |
White Solid
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| Melting Point |
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| Mol. Weight |
200.26
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| Storage |
Refrigerator, under inert atmosphere
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| Solubility |
DMSO (Slightly), Methanol (Slightly)
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| Stability |
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| Category |
Amines, Aromatics, Miscellaneous Reagents, Pharmaceuticals, Intermediates & Fine Chemicals, Sulfur & Selenium Compounds
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| Boiling Point |
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| Applications |
4-(2-Aminoethyl)benzenesulfonamide is used as the starting material in the synthesis of Des(5-methylpyrazinecarbonyl) trans-4-Methyl Glipizide (D292605); a degradation product of Glimepiride (G410150) which is a sulfonylurea hypoglycemic agent and an antidiabetic. 4-(2-Aminoethyl)benzenesulfonamide is also used as a reagent in the synthesis of deorphaning pyrrolopyrazines as potent multi-target antimalarial agents.
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| Dangerous Goods Info |
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| References |
Ratheiser, K., et al.: Arzneim.-Forsch., 43, 856, (1993); Bansal, G., et al.: J. Pharmaceut. Biomed., 43, 788 (2008); Reker, D., et al.: Angew. Chem. Int. Edit., 53, 7079 (2014)
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| Extra Notes |
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| Documents (MSDS) |
No Data Available
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| Keywords |
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