tert-Butyl 5-bromo-2-chlorobenzoate

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Reagent Code: #150571
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CAS Number 503555-23-5

science Other reagents with same CAS 503555-23-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 291.57 g/mol
Formula C₁₁H₁₂BrClO₂
badge Registry Numbers
MDL Number MFCD09800903
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the construction of complex aromatic systems. Its halogen substituents allow for selective cross-coupling reactions, such as Suzuki or Ullmann reactions, enabling the introduction of various functional groups. The tert-butyl ester group acts as a protected carboxylic acid, which can be deprotected under mild acidic conditions to release the corresponding benzoic acid derivative. This makes the compound valuable in multi-step organic syntheses where controlled reactivity and functional group compatibility are required.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,020.00
inventory 250mg
10-20 days ฿7,880.00

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tert-Butyl 5-bromo-2-chlorobenzoate
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Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the construction of complex aromatic systems. Its halogen substituents allow for selective cross-coupling reactions, such as Suzuki or Ullmann reactions, enabling the introduction of various functional groups. The tert-butyl ester group acts as a protected carboxylic acid, which can be deprotected under mild acidic conditions to release the corresponding benzoic acid derivative. This makes the compound valuable

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the construction of complex aromatic systems. Its halogen substituents allow for selective cross-coupling reactions, such as Suzuki or Ullmann reactions, enabling the introduction of various functional groups. The tert-butyl ester group acts as a protected carboxylic acid, which can be deprotected under mild acidic conditions to release the corresponding benzoic acid derivative. This makes the compound valuable in multi-step organic syntheses where controlled reactivity and functional group compatibility are required.

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