5,6-Dibromopicolinic acid
≥95%
- Product Code: 119712
CAS:
1206679-66-4
| Molecular Weight: | 280.90 g./mol | Molecular Formula: | C₆H₃Br₂NO₂ |
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| EC Number: | MDL Number: | MFCD11978042 | |
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| Density: | Storage Condition: | 2-8°C, store under inert gas |
Product Description:
5,6-Dibromopicolinic acid is primarily utilized in the field of organic synthesis as a versatile building block for the preparation of more complex chemical compounds. Its structure allows it to act as an intermediate in the synthesis of various heterocyclic compounds, which are often employed in pharmaceuticals and agrochemicals. The presence of bromine atoms in its structure makes it particularly useful in cross-coupling reactions, such as Suzuki or Heck reactions, which are pivotal in creating carbon-carbon bonds in medicinal chemistry. Additionally, it finds application in the development of ligands for metal catalysis, aiding in the production of fine chemicals and polymers. Its utility in research and development is significant, especially in the creation of novel molecules with potential biological activity.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿2,763.00 |
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| 1.000 | 10-20 days | ฿5,517.00 |
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5,6-Dibromopicolinic acid
5,6-Dibromopicolinic acid is primarily utilized in the field of organic synthesis as a versatile building block for the preparation of more complex chemical compounds. Its structure allows it to act as an intermediate in the synthesis of various heterocyclic compounds, which are often employed in pharmaceuticals and agrochemicals. The presence of bromine atoms in its structure makes it particularly useful in cross-coupling reactions, such as Suzuki or Heck reactions, which are pivotal in creating carbon-carbon bonds in medicinal chemistry. Additionally, it finds application in the development of ligands for metal catalysis, aiding in the production of fine chemicals and polymers. Its utility in research and development is significant, especially in the creation of novel molecules with potential biological activity.
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