Ethyl 3-bromo-1-methyl-1H-pyrazole-4-carboxylate
95%
- Product Code: 83641
CAS:
139308-52-4
Molecular Weight: | 233.06 g./mol | Molecular Formula: | C₇H₉BrN₂O₂ |
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EC Number: | MDL Number: | MFCD22420858 | |
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | 2-8°C, store under inert gas |
Product Description:
This chemical is primarily used in organic synthesis as a versatile building block for the construction of more complex molecules. It serves as a key intermediate in the development of pharmaceuticals, particularly in the synthesis of active pharmaceutical ingredients (APIs) that target specific biological pathways. Its structure, featuring a bromo substituent and an ester group, makes it suitable for various cross-coupling reactions, such as Suzuki or Sonogashira couplings, which are essential in drug discovery and development. Additionally, it finds application in agrochemical research for the creation of novel compounds with potential pesticidal or herbicidal properties. Its reactivity and functional groups allow for further modifications, enabling the exploration of diverse chemical spaces in both medicinal and agricultural chemistry.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.100 | 10-20 days | $180.48 |
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0.250 | 10-20 days | $315.74 |
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1.000 | 10-20 days | $631.48 |
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Ethyl 3-bromo-1-methyl-1H-pyrazole-4-carboxylate
This chemical is primarily used in organic synthesis as a versatile building block for the construction of more complex molecules. It serves as a key intermediate in the development of pharmaceuticals, particularly in the synthesis of active pharmaceutical ingredients (APIs) that target specific biological pathways. Its structure, featuring a bromo substituent and an ester group, makes it suitable for various cross-coupling reactions, such as Suzuki or Sonogashira couplings, which are essential in drug discovery and development. Additionally, it finds application in agrochemical research for the creation of novel compounds with potential pesticidal or herbicidal properties. Its reactivity and functional groups allow for further modifications, enabling the exploration of diverse chemical spaces in both medicinal and agricultural chemistry.
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