2-(3-Bromo-2-methoxyphenyl)acetonitrile

97%

Reagent Code: #152485
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CAS Number 1261602-72-5

science Other reagents with same CAS 1261602-72-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 226.07 g/mol
Formula C₉H₈BrNO
badge Registry Numbers
MDL Number MFCD18391932
inventory_2 Storage & Handling
Storage 2-8°C, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the production of active pharmaceutical ingredients (APIs) that require substituted phenylacetonitrile derivatives. Its bromo and methoxy functional groups allow for selective cross-coupling reactions, making it valuable in constructing complex organic molecules. Commonly employed in the development of central nervous system (CNS) agents and anti-inflammatory compounds due to its ability to modulate biological activity when incorporated into larger structures. Also utilized in research settings for the preparation of novel heterocyclic compounds through cyclization and nucleophilic substitution reactions.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿1,850.00
250mg
10-20 days ฿3,120.00
1g
10-20 days ฿8,390.00
5g
10-20 days ฿32,890.00
2-(3-Bromo-2-methoxyphenyl)acetonitrile
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the production of active pharmaceutical ingredients (APIs) that require substituted phenylacetonitrile derivatives. Its bromo and methoxy functional groups allow for selective cross-coupling reactions, making it valuable in constructing complex organic molecules. Commonly employed in the development of central nervous system (CNS) agents and anti-inflammatory compounds due to its ability to modulate biological activity when i

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the production of active pharmaceutical ingredients (APIs) that require substituted phenylacetonitrile derivatives. Its bromo and methoxy functional groups allow for selective cross-coupling reactions, making it valuable in constructing complex organic molecules. Commonly employed in the development of central nervous system (CNS) agents and anti-inflammatory compounds due to its ability to modulate biological activity when incorporated into larger structures. Also utilized in research settings for the preparation of novel heterocyclic compounds through cyclization and nucleophilic substitution reactions.

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