1-Bromo-2-chloro-5-fluoro-4-nitrobenzene

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Reagent Code: #146246
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CAS Number 1027833-17-5

science Other reagents with same CAS 1027833-17-5

blur_circular Chemical Specifications

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Weight 254.44 g/mol
Formula C₆H₂BrClFNO₂
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of fluorinated and nitro-substituted aromatic compounds. Its halogen and nitro functional groups allow for selective cross-coupling reactions, making it valuable in the preparation of complex organic molecules. Commonly employed in the manufacture of dyes, pigments, and specialty polymers where electron-withdrawing substituents enhance stability and reactivity. Also utilized in research settings for the construction of heterocyclic systems through nucleophilic substitution or reduction pathways.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿2,280.00
inventory 10g
10-20 days ฿3,190.00
inventory 25g
10-20 days ฿7,960.00
inventory 100g
10-20 days ฿31,800.00

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1-Bromo-2-chloro-5-fluoro-4-nitrobenzene
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Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of fluorinated and nitro-substituted aromatic compounds. Its halogen and nitro functional groups allow for selective cross-coupling reactions, making it valuable in the preparation of complex organic molecules. Commonly employed in the manufacture of dyes, pigments, and specialty polymers where electron-withdrawing substituents enhance stability and reactivity. Also utilized in research settings fo
Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of fluorinated and nitro-substituted aromatic compounds. Its halogen and nitro functional groups allow for selective cross-coupling reactions, making it valuable in the preparation of complex organic molecules. Commonly employed in the manufacture of dyes, pigments, and specialty polymers where electron-withdrawing substituents enhance stability and reactivity. Also utilized in research settings for the construction of heterocyclic systems through nucleophilic substitution or reduction pathways.
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