(2-Chloro-pyridin-3-yl)-carbamic acid tert-butyl ester
95%
- Product Code: 82839
CAS:
209798-48-1
Molecular Weight: | 228.68 g./mol | Molecular Formula: | C₁₀H₁₃ClN₂O₂ |
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EC Number: | MDL Number: | MFCD12026344 | |
Melting Point: | Boiling Point: | 279.6±25.0 °C(Predicted) | |
Density: | Storage Condition: | room temperature |
Product Description:
This chemical is primarily utilized in the field of organic synthesis as an intermediate in the production of more complex compounds. It is often employed in the development of pharmaceuticals, particularly in the synthesis of active pharmaceutical ingredients (APIs) that require pyridine derivatives. Its structure, featuring a chloro and carbamic acid tert-butyl ester group, makes it a valuable building block for constructing molecules with specific biological activities. Additionally, it is used in research and development for creating novel compounds that may have potential applications in medicinal chemistry, such as inhibitors or modulators of biological targets. Its stability and reactivity under various conditions make it a versatile reagent in synthetic organic chemistry.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.250 | 10-20 days | ฿918.00 |
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1.000 | 10-20 days | ฿2,628.00 |
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5.000 | 10-20 days | ฿8,658.00 |
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(2-Chloro-pyridin-3-yl)-carbamic acid tert-butyl ester
This chemical is primarily utilized in the field of organic synthesis as an intermediate in the production of more complex compounds. It is often employed in the development of pharmaceuticals, particularly in the synthesis of active pharmaceutical ingredients (APIs) that require pyridine derivatives. Its structure, featuring a chloro and carbamic acid tert-butyl ester group, makes it a valuable building block for constructing molecules with specific biological activities. Additionally, it is used in research and development for creating novel compounds that may have potential applications in medicinal chemistry, such as inhibitors or modulators of biological targets. Its stability and reactivity under various conditions make it a versatile reagent in synthetic organic chemistry.
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