5-Bromo-2-methylbenzaldehyde

97%

Reagent Code: #146040
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CAS Number 90050-59-2

science Other reagents with same CAS 90050-59-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 199.05 g/mol
Formula C₈H₇BrO
badge Registry Numbers
MDL Number MFCD05662390
inventory_2 Storage & Handling
Storage 2-8°C, inert gas atmosphere

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) for drugs targeting inflammation and central nervous system disorders. It serves as a building block in organic reactions, especially in cross-coupling reactions like Suzuki and Heck couplings, enabling the formation of carbon-carbon bonds for complex molecule assembly. Also employed in the production of agrochemicals, such as herbicides and fungicides, due to its reactivity and functional group compatibility. Its bromine and aldehyde functionalities allow for selective modifications, making it valuable in research and development of new bioactive compounds.

Available Sizes & Pricing

Size Availability Unit Price Quantity
5g
10-20 days ฿2,690.00
10g
10-20 days ฿4,480.00
5-Bromo-2-methylbenzaldehyde
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) for drugs targeting inflammation and central nervous system disorders. It serves as a building block in organic reactions, especially in cross-coupling reactions like Suzuki and Heck couplings, enabling the formation of carbon-carbon bonds for complex molecule assembly. Also employed in the production of agrochemicals, such as herbicides and fungicides, due to its re

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) for drugs targeting inflammation and central nervous system disorders. It serves as a building block in organic reactions, especially in cross-coupling reactions like Suzuki and Heck couplings, enabling the formation of carbon-carbon bonds for complex molecule assembly. Also employed in the production of agrochemicals, such as herbicides and fungicides, due to its reactivity and functional group compatibility. Its bromine and aldehyde functionalities allow for selective modifications, making it valuable in research and development of new bioactive compounds.

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