Ethyl 5-bromo-6-chloropicolinate

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Reagent Code: #182817
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CAS Number 1214337-57-1

science Other reagents with same CAS 1214337-57-1

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Weight 264.5 g/mol
Formula C₈H₇BrClNO₂
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of agrochemicals, particularly herbicides and insecticides, due to the presence of reactive halogen atoms that allow further functionalization. The ester group enables coupling reactions or hydrolysis to modify solubility and reactivity. Commonly employed in the development of pyridine-based crop protection agents where selective halogen substitution enhances biological activity. Also utilized in medicinal chemistry for constructing heterocyclic compounds with potential bioactive properties. Its structure supports cross-coupling reactions like Suzuki or Heck, making it valuable in creating complex molecules for research and industrial applications.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,190.00
inventory 1g
10-20 days ฿3,620.00
inventory 5g
10-20 days ฿7,940.00
inventory 25g
10-20 days ฿38,420.00
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Ethyl 5-bromo-6-chloropicolinate
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Used as a key intermediate in the synthesis of agrochemicals, particularly herbicides and insecticides, due to the presence of reactive halogen atoms that allow further functionalization. The ester group enables coupling reactions or hydrolysis to modify solubility and reactivity. Commonly employed in the development of pyridine-based crop protection agents where selective halogen substitution enhances biological activity. Also utilized in medicinal chemistry for constructing heterocyclic compounds with

Used as a key intermediate in the synthesis of agrochemicals, particularly herbicides and insecticides, due to the presence of reactive halogen atoms that allow further functionalization. The ester group enables coupling reactions or hydrolysis to modify solubility and reactivity. Commonly employed in the development of pyridine-based crop protection agents where selective halogen substitution enhances biological activity. Also utilized in medicinal chemistry for constructing heterocyclic compounds with potential bioactive properties. Its structure supports cross-coupling reactions like Suzuki or Heck, making it valuable in creating complex molecules for research and industrial applications.

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