Description
Dimethylsulfamoyl Chloride CAS 13360-57-1 Quick Details
| Chemical Name: | Dimethylsulfamoyl Chloride |
| Other Name: | N,N-Dimethylsulfamoyl chloride; Dimethylsulfamoylchloride |
| CAS: | 13360-57-1 |
| EINECS: | 236-412-4 |
| Type: | Agricultural raw materials; Intermediates of synthetic materials; Pharmaceutical raw materials; Organic raw materials |
| Molecular Formula: | C2H6ClNO2S |
| Molecular Weight: | 143.59 |
Chemical Properties
| Melting point | -13 °C |
| Boiling point | 114 °C75 mm Hg(lit.) |
| density | 1.337 g/mL at 25 °C(lit.) |
| refractive index | n20/D 1.452(lit.) |
| Fp | 202 °F |
| storage temp. | Inert atmosphere,2-8°C |
| pka | -8.25±0.70(Predicted) |
| Water Solubility | DECOMPOSES |
Uses of Dimethylsulfamoyl Chloride
Dimethylsulfamoyl chloride is a key synthetic intermediate in organic chemistry. It is used in agrochemicals, pharmaceuticals, and polymers due to its unique sulfonyl functional group. This compound exhibits a variety of biological activities, making it significant in the production of medicines and pesticides.
Dimethylsulfamoyl chloride has pharmacological properties that help treat various diseases. Its anti-tumor, anti-schizophrenia, anti-inflammatory, and antibacterial effects contribute to its therapeutic value. The 4-position and 3-position of the molecule can be easily modified, which enhances its versatility in synthesis. Moreover, it is relatively easy and inexpensive to produce.
Compounds containing dimethylsulfamoyl chloride often have large conjugated systems, leading to excellent photoelectric properties and strong fluorescence. These characteristics make them suitable for use in organic coatings for OLED screens, offering advantages such as thinness, energy efficiency, and high luminous output. They are also important in light-emitting diodes and semiconductors.
In addition, N,N-dimethylsulfamoyl chloride is effective for synthesizing sulfonamides, which are crucial in medicine. Sulfonamides derived from aminotetralin and acetylcholinesterase inhibitors serve as anticancer agents. The compound is also utilized for esterification and amidation reactions, such as in the synthesis of coumarin.
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