5-Cyano-2-bromobenzaldehyde

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Reagent Code: #172949
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CAS Number 89003-95-2

science Other reagents with same CAS 89003-95-2

blur_circular Chemical Specifications

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Weight 210.03 g/mol
Formula C₈H₄BrNO
badge Registry Numbers
MDL Number MFCD11858309
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of heterocyclic compounds. Its functional groups—cyano, bromo, and aldehyde—allow for diverse chemical transformations, such as cross-coupling reactions, nucleophilic substitutions, and condensation reactions. Commonly employed in the preparation of benzoxazoles, benzimidazoles, and other nitrogen-containing fused rings with biological activity. Also utilized in the manufacture of dyes and functional materials due to its electron-withdrawing substituents and reactivity profile.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿800.00
inventory 1g
10-20 days ฿2,400.00
inventory 5g
10-20 days ฿8,000.00

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5-Cyano-2-bromobenzaldehyde
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Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of heterocyclic compounds. Its functional groups—cyano, bromo, and aldehyde—allow for diverse chemical transformations, such as cross-coupling reactions, nucleophilic substitutions, and condensation reactions. Commonly employed in the preparation of benzoxazoles, benzimidazoles, and other nitrogen-containing fused rings with biological activity. Also utilized in the manufacture of dyes and fu

Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of heterocyclic compounds. Its functional groups—cyano, bromo, and aldehyde—allow for diverse chemical transformations, such as cross-coupling reactions, nucleophilic substitutions, and condensation reactions. Commonly employed in the preparation of benzoxazoles, benzimidazoles, and other nitrogen-containing fused rings with biological activity. Also utilized in the manufacture of dyes and functional materials due to its electron-withdrawing substituents and reactivity profile.

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