Diethyl (4-chloropyridine-2,6-diyl)dicarbamate
95%
- Product Code: 82890
CAS:
63708-78-1
Molecular Weight: | 287.70 g./mol | Molecular Formula: | C₁₁H₁₄ClN₃O₄ |
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EC Number: | MDL Number: | MFCD30598628 | |
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | 2-8°C |
Product Description:
This chemical is primarily utilized in the field of organic synthesis, where it serves as an intermediate in the production of more complex molecules. Its structure, featuring a 4-chloropyridine core, makes it valuable for constructing compounds with potential biological activity. It is often employed in the development of pharmaceuticals, particularly in the synthesis of drugs targeting specific enzymes or receptors. Additionally, its dicarbamate functionality allows it to participate in various chemical reactions, such as coupling or condensation, enabling the creation of diverse chemical entities. Researchers also explore its use in agrochemical research for designing novel pesticides or herbicides, leveraging its pyridine moiety for interaction with biological targets.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.100 | 10-20 days | ฿9,360.00 |
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0.250 | 10-20 days | ฿17,550.00 |
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1.000 | 10-20 days | ฿36,000.00 |
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Diethyl (4-chloropyridine-2,6-diyl)dicarbamate
This chemical is primarily utilized in the field of organic synthesis, where it serves as an intermediate in the production of more complex molecules. Its structure, featuring a 4-chloropyridine core, makes it valuable for constructing compounds with potential biological activity. It is often employed in the development of pharmaceuticals, particularly in the synthesis of drugs targeting specific enzymes or receptors. Additionally, its dicarbamate functionality allows it to participate in various chemical reactions, such as coupling or condensation, enabling the creation of diverse chemical entities. Researchers also explore its use in agrochemical research for designing novel pesticides or herbicides, leveraging its pyridine moiety for interaction with biological targets.
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