Methyl 3-amino-4,6-dibromopicolinate

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Reagent Code: #203136
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CAS Number 2402828-54-8

science Other reagents with same CAS 2402828-54-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 309.94 g/mol
Formula C₇H₆Br₂N₂O₂
badge Registry Numbers
MDL Number MFCD32219505
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used as a key intermediate in the synthesis of agrochemicals, particularly herbicides and plant growth regulators. Its brominated structure enables selective reactivity in coupling reactions, making it valuable in the development of bromine-containing active ingredients. It also serves in pharmaceutical research for constructing nitrogen- and halogen-functionalized heterocycles, which are important in drug design. The amine and ester groups allow for easy modification, facilitating the creation of derivative compounds for biological screening.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,790.00
inventory 250mg
10-20 days ฿4,100.00
inventory 1g
10-20 days ฿15,300.00
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Methyl 3-amino-4,6-dibromopicolinate
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Used as a key intermediate in the synthesis of agrochemicals, particularly herbicides and plant growth regulators. Its brominated structure enables selective reactivity in coupling reactions, making it valuable in the development of bromine-containing active ingredients. It also serves in pharmaceutical research for constructing nitrogen- and halogen-functionalized heterocycles, which are important in drug design. The amine and ester groups allow for easy modification, facilitating the creation of deriva

Used as a key intermediate in the synthesis of agrochemicals, particularly herbicides and plant growth regulators. Its brominated structure enables selective reactivity in coupling reactions, making it valuable in the development of bromine-containing active ingredients. It also serves in pharmaceutical research for constructing nitrogen- and halogen-functionalized heterocycles, which are important in drug design. The amine and ester groups allow for easy modification, facilitating the creation of derivative compounds for biological screening.

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