6-(Methylsulfonyl)pyridin-3-amine
≥95%
- Product Code: 120429
CAS:
187143-22-2
Molecular Weight: | 172.21 g./mol | Molecular Formula: | C₆H₈N₂O₂S |
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EC Number: | MDL Number: | MFCD09941635 | |
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | Room temperature, away from light, stored in an inert gas |
Product Description:
6-(Methylsulfonyl)pyridin-3-amine is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various pharmaceutical compounds. Its structure, featuring a sulfonyl group and an amine group attached to a pyridine ring, makes it a valuable building block for developing molecules with potential therapeutic properties. It is often employed in the creation of inhibitors targeting specific enzymes or receptors, particularly in the development of drugs for treating inflammatory diseases, cancers, and neurological disorders. Additionally, its unique chemical properties allow it to participate in diverse organic reactions, facilitating the design of novel bioactive compounds with enhanced efficacy and selectivity.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.100 | 10-20 days | ฿5,184.00 |
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0.250 | 10-20 days | ฿9,072.00 |
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1.000 | 10-20 days | ฿20,421.00 |
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6-(Methylsulfonyl)pyridin-3-amine
6-(Methylsulfonyl)pyridin-3-amine is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various pharmaceutical compounds. Its structure, featuring a sulfonyl group and an amine group attached to a pyridine ring, makes it a valuable building block for developing molecules with potential therapeutic properties. It is often employed in the creation of inhibitors targeting specific enzymes or receptors, particularly in the development of drugs for treating inflammatory diseases, cancers, and neurological disorders. Additionally, its unique chemical properties allow it to participate in diverse organic reactions, facilitating the design of novel bioactive compounds with enhanced efficacy and selectivity.
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