4-(2-Aminoethyl)benzenesulfonamide
99%
- Product Code: 110609
Alias:
4-(2-aminoethyl)benzenesulfonamide
CAS:
35303-76-5
| Molecular Weight: | 200.26 g./mol | Molecular Formula: | H₂NCH₂CH₂C₆H₄SO₂NH₂ |
|---|---|---|---|
| EC Number: | 252-501-0 | MDL Number: | MFCD00010301 |
| Melting Point: | 150-152 °C(lit.) | Boiling Point: | |
| Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in the field of medicinal chemistry and pharmaceutical research. It serves as a key intermediate in the synthesis of various sulfonamide-based drugs, which are widely used as antibiotics, diuretics, and anti-inflammatory agents. Its structure allows for modifications that can enhance the efficacy and specificity of the resulting drugs. Additionally, it is employed in biochemical studies to investigate enzyme inhibition mechanisms, particularly those involving carbonic anhydrase, due to its sulfonamide functional group. Its applications also extend to the development of diagnostic agents and in the study of cellular processes related to ion transport and pH regulation.
Product Specification:
| Test | Specification |
|---|---|
| Loss On Drying | 0-1.5 |
| Melting Point | 145-150 |
| Purity | 99-100 |
| Water By Karl Fischer | 0-1 |
| Appearance | White To Yellow Crystals Or Powder Or Crystalline Powder |
| Infrared Spectrum | Conforms To Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 5.000 | 10-20 days | ฿300.00 |
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| 25.000 | 10-20 days | ฿580.00 |
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| 100.000 | 10-20 days | ฿2,200.00 |
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| 500.000 | 10-20 days | ฿10,120.00 |
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4-(2-Aminoethyl)benzenesulfonamide
This compound is primarily utilized in the field of medicinal chemistry and pharmaceutical research. It serves as a key intermediate in the synthesis of various sulfonamide-based drugs, which are widely used as antibiotics, diuretics, and anti-inflammatory agents. Its structure allows for modifications that can enhance the efficacy and specificity of the resulting drugs. Additionally, it is employed in biochemical studies to investigate enzyme inhibition mechanisms, particularly those involving carbonic anhydrase, due to its sulfonamide functional group. Its applications also extend to the development of diagnostic agents and in the study of cellular processes related to ion transport and pH regulation.
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