3-Bromo-5-hydroxybenzonitrile

98%

Reagent Code: #65610
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CAS Number 770718-92-8

science Other reagents with same CAS 770718-92-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 198.02 g/mol
Formula C₇H₄BrNO
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used primarily in organic synthesis, this compound serves as a key intermediate in the production of various pharmaceuticals and agrochemicals. Its bromo and hydroxy functional groups make it versatile for further chemical modifications, such as coupling reactions or substitutions, enabling the creation of complex molecules. In pharmaceuticals, it is often employed in the development of active ingredients targeting specific biological pathways. Additionally, its nitrile group can be hydrolyzed to form carboxylic acids or reduced to amines, expanding its utility in synthesizing diverse chemical structures. In agrochemicals, it contributes to the formulation of herbicides or pesticides by acting as a building block for active compounds. Its stability and reactivity make it a valuable component in research and industrial applications.

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Test Parameter Specification
Appearance Off-White Powder
Purity (%) 97.5-100
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿3,555.00
inventory 50mg
10-20 days ฿1,170.00

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3-Bromo-5-hydroxybenzonitrile
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Used primarily in organic synthesis, this compound serves as a key intermediate in the production of various pharmaceuticals and agrochemicals. Its bromo and hydroxy functional groups make it versatile for further chemical modifications, such as coupling reactions or substitutions, enabling the creation of complex molecules. In pharmaceuticals, it is often employed in the development of active ingredients targeting specific biological pathways. Additionally, its nitrile group can be hydrolyzed to form carbo
Used primarily in organic synthesis, this compound serves as a key intermediate in the production of various pharmaceuticals and agrochemicals. Its bromo and hydroxy functional groups make it versatile for further chemical modifications, such as coupling reactions or substitutions, enabling the creation of complex molecules. In pharmaceuticals, it is often employed in the development of active ingredients targeting specific biological pathways. Additionally, its nitrile group can be hydrolyzed to form carboxylic acids or reduced to amines, expanding its utility in synthesizing diverse chemical structures. In agrochemicals, it contributes to the formulation of herbicides or pesticides by acting as a building block for active compounds. Its stability and reactivity make it a valuable component in research and industrial applications.
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