1-(4-Hydrazinylphenyl)-N-methylmethanesulfonamide hydrochloride
97%
- Product Code: 119659
CAS:
88933-16-8
| Molecular Weight: | 251.73 g./mol | Molecular Formula: | C₈H₁₄ClN₃O₂S |
|---|---|---|---|
| EC Number: | MDL Number: | ||
| Melting Point: | 170-173°C | Boiling Point: | 448.8°C |
| Density: | Storage Condition: | 2-8°C |
Product Description:
This compound is primarily utilized in pharmaceutical research and development, particularly in the synthesis of biologically active molecules. It serves as a key intermediate in the creation of compounds that target specific enzymes or receptors, often in the context of drug discovery for conditions such as inflammation, cancer, or neurological disorders. Its hydrazine moiety makes it valuable for constructing hydrazone derivatives, which are frequently explored for their therapeutic potential. Additionally, it may be employed in the development of chemical probes or inhibitors for studying biochemical pathways. Its sulfonamide group further enhances its utility in medicinal chemistry due to its ability to interact with biological targets.
Product Specification:
| Test | Specification |
|---|---|
| Appearance | White To Off-White Powder Or Crystals |
| Purity (%) | 96.5-100 |
| Infrared Spectrum | Conforms To Structure |
| NMR | Conforms To Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿300.00 |
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| 1.000 | 10-20 days | ฿360.00 |
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| 5.000 | 10-20 days | ฿610.00 |
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| 25.000 | 10-20 days | ฿1,600.00 |
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1-(4-Hydrazinylphenyl)-N-methylmethanesulfonamide hydrochloride
This compound is primarily utilized in pharmaceutical research and development, particularly in the synthesis of biologically active molecules. It serves as a key intermediate in the creation of compounds that target specific enzymes or receptors, often in the context of drug discovery for conditions such as inflammation, cancer, or neurological disorders. Its hydrazine moiety makes it valuable for constructing hydrazone derivatives, which are frequently explored for their therapeutic potential. Additionally, it may be employed in the development of chemical probes or inhibitors for studying biochemical pathways. Its sulfonamide group further enhances its utility in medicinal chemistry due to its ability to interact with biological targets.
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