methyl 3-bromo-4-chloro-5-nitrobenzoate

≥95%

Reagent Code: #214127
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CAS Number 1504888-15-6

science Other reagents with same CAS 1504888-15-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 294.49 g/mol
Formula C₈H₅BrClNO₄
badge Registry Numbers
MDL Number MFCD24107080
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry, light-proof

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of bioactive molecules that require substituted benzoate derivatives. Its functional groups—bromine, chlorine, and nitro—allow for sequential substitution reactions, making it valuable in multi-step organic synthesis. Commonly employed in the preparation of antimicrobial agents, herbicides, and dyes due to its reactivity and ability to serve as a building block in cross-coupling reactions.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿6,310.00
inventory 250mg
10-20 days ฿10,700.00
inventory 1g
10-20 days ฿28,820.00
inventory 5g
10-20 days ฿100,790.00

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methyl 3-bromo-4-chloro-5-nitrobenzoate
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Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of bioactive molecules that require substituted benzoate derivatives. Its functional groups—bromine, chlorine, and nitro—allow for sequential substitution reactions, making it valuable in multi-step organic synthesis. Commonly employed in the preparation of antimicrobial agents, herbicides, and dyes due to its reactivity and ability to serve as a building block in cross-coupling reactions.

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of bioactive molecules that require substituted benzoate derivatives. Its functional groups—bromine, chlorine, and nitro—allow for sequential substitution reactions, making it valuable in multi-step organic synthesis. Commonly employed in the preparation of antimicrobial agents, herbicides, and dyes due to its reactivity and ability to serve as a building block in cross-coupling reactions.

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