4-bromo-N-[(2-methoxyphenyl)methyl]benzenesulfonamide
95%
- Product Code: 124319
CAS:
349404-81-5
| Molecular Weight: | 356.23 g./mol | Molecular Formula: | C₁₄H₁₄BrNO₃S |
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| EC Number: | MDL Number: | MFCD01215051 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in the field of medicinal chemistry as an intermediate in the synthesis of more complex molecules. It is often employed in the development of potential pharmaceutical agents, particularly those targeting specific enzymes or receptors in the body. Its structure, which includes a bromo and sulfonamide group, makes it a valuable building block for creating compounds with potential anti-inflammatory, antimicrobial, or anticancer properties. Researchers also explore its use in designing inhibitors for various biological pathways, contributing to drug discovery and development efforts. Additionally, it may serve as a key component in organic synthesis for constructing novel chemical entities with tailored biological activities.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿2,988.00 |
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| 0.250 | 10-20 days | ฿4,329.00 |
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| 1.000 | 10-20 days | ฿10,944.00 |
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4-bromo-N-[(2-methoxyphenyl)methyl]benzenesulfonamide
This compound is primarily utilized in the field of medicinal chemistry as an intermediate in the synthesis of more complex molecules. It is often employed in the development of potential pharmaceutical agents, particularly those targeting specific enzymes or receptors in the body. Its structure, which includes a bromo and sulfonamide group, makes it a valuable building block for creating compounds with potential anti-inflammatory, antimicrobial, or anticancer properties. Researchers also explore its use in designing inhibitors for various biological pathways, contributing to drug discovery and development efforts. Additionally, it may serve as a key component in organic synthesis for constructing novel chemical entities with tailored biological activities.
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