5,6-Dibromopicolinic acid

≥95%

Reagent Code: #119712
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CAS Number 1206679-66-4

science Other reagents with same CAS 1206679-66-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 280.90 g/mol
Formula C₆H₃Br₂NO₂
badge Registry Numbers
MDL Number MFCD11978042
inventory_2 Storage & Handling
Storage 2-8°C, store under inert gas

description 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.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿2,763.00
inventory 1g
10-20 days ฿5,517.00

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5,6-Dibromopicolinic acid
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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-

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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