Methyl 3-bromo-5-fluoroisonicotinate

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Reagent Code: #207267
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CAS Number 1214325-21-9

science Other reagents with same CAS 1214325-21-9

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Weight 234.02 g/mol
Formula C₇H₅BrFNO₂
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MDL Number MFCD14698118
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other bioactive molecules. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for constructing complex heterocyclic compounds. Commonly employed in cross-coupling reactions to introduce fluorinated and brominated pyridine motifs, which are prevalent in agrochemicals and drug candidates. Also utilized in research settings for the preparation of fluorescent probes and labeled compounds due to the reactivity of the bromo and ester groups.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,990.00
inventory 1g
10-20 days ฿5,430.00
inventory 5g
10-20 days ฿25,480.00

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Methyl 3-bromo-5-fluoroisonicotinate
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other bioactive molecules. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for constructing complex heterocyclic compounds. Commonly employed in cross-coupling reactions to introduce fluorinated and brominated pyridine motifs, which are prevalent in agrochemicals and drug candidates. Also utilized in research settings for the preparation

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other bioactive molecules. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for constructing complex heterocyclic compounds. Commonly employed in cross-coupling reactions to introduce fluorinated and brominated pyridine motifs, which are prevalent in agrochemicals and drug candidates. Also utilized in research settings for the preparation of fluorescent probes and labeled compounds due to the reactivity of the bromo and ester groups.

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