4-Bromo-3-hydroxybenzonitrile

95%

Reagent Code: #65608
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CAS Number 916213-60-0

science Other reagents with same CAS 916213-60-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 198.02 g/mol
Formula C₇H₄BrNO
badge Registry Numbers
MDL Number MFCD16999194
inventory_2 Storage & Handling
Storage Room temperature, sealed, dry

description Product Description

Used primarily in organic synthesis, this compound serves as a key intermediate in the production of pharmaceuticals and agrochemicals. Its bromine and nitrile functional groups make it versatile for further chemical modifications, enabling the creation of complex molecules. It is often employed in cross-coupling reactions, such as Suzuki or Sonogashira couplings, to construct biologically active compounds. Additionally, it finds utility in the development of herbicides and fungicides, contributing to crop protection strategies. Its hydroxyl group also allows for derivatization, enhancing its role in synthesizing specialty chemicals.

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Test Parameter Specification
Purity 95-100
Appearance White to yellow crystal-powder

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿8,541.00

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4-Bromo-3-hydroxybenzonitrile
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Used primarily in organic synthesis, this compound serves as a key intermediate in the production of pharmaceuticals and agrochemicals. Its bromine and nitrile functional groups make it versatile for further chemical modifications, enabling the creation of complex molecules. It is often employed in cross-coupling reactions, such as Suzuki or Sonogashira couplings, to construct biologically active compounds. Additionally, it finds utility in the development of herbicides and fungicides, contributing to cr

Used primarily in organic synthesis, this compound serves as a key intermediate in the production of pharmaceuticals and agrochemicals. Its bromine and nitrile functional groups make it versatile for further chemical modifications, enabling the creation of complex molecules. It is often employed in cross-coupling reactions, such as Suzuki or Sonogashira couplings, to construct biologically active compounds. Additionally, it finds utility in the development of herbicides and fungicides, contributing to crop protection strategies. Its hydroxyl group also allows for derivatization, enhancing its role in synthesizing specialty chemicals.

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