3-Bromo-5-methoxybenzonitrile

98%

Reagent Code: #65555
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CAS Number 867366-91-4

science Other reagents with same CAS 867366-91-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 212.04 g/mol
Formula C₈H₆BrNO
badge Registry Numbers
MDL Number MFCD08061971
thermostat Physical Properties
Boiling Point 253.5°C
inventory_2 Storage & Handling
Storage room temperature, dry

description Product Description

This chemical is primarily utilized in organic synthesis as a versatile intermediate. It serves as a building block in the preparation of various pharmaceuticals, agrochemicals, and specialty chemicals. Its bromo and nitrile functional groups make it a valuable precursor for cross-coupling reactions, such as Suzuki or Sonogashira couplings, enabling the creation of complex molecular structures. Additionally, the methoxy group enhances its reactivity in electrophilic substitution reactions, making it useful in the development of biologically active compounds. It is also employed in research and development for designing new materials and ligands in coordination chemistry.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿297.00
inventory 1g
10-20 days ฿927.00

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3-Bromo-5-methoxybenzonitrile
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This chemical is primarily utilized in organic synthesis as a versatile intermediate. It serves as a building block in the preparation of various pharmaceuticals, agrochemicals, and specialty chemicals. Its bromo and nitrile functional groups make it a valuable precursor for cross-coupling reactions, such as Suzuki or Sonogashira couplings, enabling the creation of complex molecular structures. Additionally, the methoxy group enhances its reactivity in electrophilic substitution reactions, making it usef

This chemical is primarily utilized in organic synthesis as a versatile intermediate. It serves as a building block in the preparation of various pharmaceuticals, agrochemicals, and specialty chemicals. Its bromo and nitrile functional groups make it a valuable precursor for cross-coupling reactions, such as Suzuki or Sonogashira couplings, enabling the creation of complex molecular structures. Additionally, the methoxy group enhances its reactivity in electrophilic substitution reactions, making it useful in the development of biologically active compounds. It is also employed in research and development for designing new materials and ligands in coordination chemistry.

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