5-methoxy-1-(4-methylbenzenesulfonyl)-1H-indole
97%
- Product Code: 48437
CAS:
139717-71-8
Molecular Weight: | 301.3602 g./mol | Molecular Formula: | C₁₆H₁₅NO₃S |
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EC Number: | MDL Number: | ||
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | 2-8℃, dry |
Product Description:
This compound is primarily utilized in the field of medicinal chemistry as an intermediate in the synthesis of more complex molecules, particularly those with potential pharmacological activities. Its structure, featuring an indole core and a sulfonyl group, makes it a valuable building block for developing compounds that may interact with biological targets such as receptors or enzymes. Researchers often explore its derivatives for their potential anti-inflammatory, anticancer, or antimicrobial properties. Additionally, it can be employed in organic synthesis to create novel heterocyclic compounds, which are of interest in drug discovery and development. Its role in facilitating the creation of diverse chemical libraries aids in the identification of new therapeutic agents.
Product Specification:
Test | Specification |
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APPEARANCE | Orange Powder |
PURITY | 96.5-100 |
Infrared spectrum | Conforms to Structure |
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.050 | 10-20 days | ฿2,800.00 |
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0.250 | 10-20 days | ฿8,010.00 |
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1.000 | 10-20 days | ฿24,400.00 |
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5-methoxy-1-(4-methylbenzenesulfonyl)-1H-indole
This compound is primarily utilized in the field of medicinal chemistry as an intermediate in the synthesis of more complex molecules, particularly those with potential pharmacological activities. Its structure, featuring an indole core and a sulfonyl group, makes it a valuable building block for developing compounds that may interact with biological targets such as receptors or enzymes. Researchers often explore its derivatives for their potential anti-inflammatory, anticancer, or antimicrobial properties. Additionally, it can be employed in organic synthesis to create novel heterocyclic compounds, which are of interest in drug discovery and development. Its role in facilitating the creation of diverse chemical libraries aids in the identification of new therapeutic agents.
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