(4-Bromo-2-methoxyphenyl)acetonitrile

95%

Reagent Code: #81346
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CAS Number 858523-37-2

science Other reagents with same CAS 858523-37-2

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scatter_plot Molecular Information
Weight 226.07 g/mol
Formula C₉H₈BrNO
badge Registry Numbers
MDL Number MFCD11847504
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of compounds with potential therapeutic properties. It plays a role in the production of agrochemicals, aiding in the creation of pesticides or herbicides. Additionally, it is utilized in organic chemistry research for the construction of complex molecules, often in the formation of heterocyclic compounds. Its bromo and nitrile groups make it a versatile building block in various chemical reactions, including nucleophilic substitutions and cyclizations.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿999.00
inventory 1g
10-20 days ฿1,485.00

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(4-Bromo-2-methoxyphenyl)acetonitrile
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of compounds with potential therapeutic properties. It plays a role in the production of agrochemicals, aiding in the creation of pesticides or herbicides. Additionally, it is utilized in organic chemistry research for the construction of complex molecules, often in the formation of heterocyclic compounds. Its bromo and nitrile groups make it a versatile building block in various chemical reactions, including nuc

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of compounds with potential therapeutic properties. It plays a role in the production of agrochemicals, aiding in the creation of pesticides or herbicides. Additionally, it is utilized in organic chemistry research for the construction of complex molecules, often in the formation of heterocyclic compounds. Its bromo and nitrile groups make it a versatile building block in various chemical reactions, including nucleophilic substitutions and cyclizations.

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