2-Bromo-4-chloro-N-methoxy-N-methylbenzamide

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Reagent Code: #151393
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CAS Number 1255099-63-8

science Other reagents with same CAS 1255099-63-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 278.53 g/mol
Formula C₉H₉BrClNO₂
badge Registry Numbers
MDL Number MFCD17926350
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) for central nervous system (CNS) drugs. It serves as a building block in the preparation of selective kinase inhibitors and other bioactive molecules due to its ability to undergo palladium-catalyzed cross-coupling reactions. Its structure allows for efficient derivatization, making it valuable in medicinal chemistry for optimizing drug potency and metabolic stability. Also employed in research settings for the design of novel anti-inflammatory and anticancer agents.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿770.00
inventory 1g
10-20 days ฿2,060.00
inventory 5g
10-20 days ฿7,780.00

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2-Bromo-4-chloro-N-methoxy-N-methylbenzamide
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) for central nervous system (CNS) drugs. It serves as a building block in the preparation of selective kinase inhibitors and other bioactive molecules due to its ability to undergo palladium-catalyzed cross-coupling reactions. Its structure allows for efficient derivatization, making it valuable in medicinal chemistry for optimizing drug potency and metabolic stabilit

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) for central nervous system (CNS) drugs. It serves as a building block in the preparation of selective kinase inhibitors and other bioactive molecules due to its ability to undergo palladium-catalyzed cross-coupling reactions. Its structure allows for efficient derivatization, making it valuable in medicinal chemistry for optimizing drug potency and metabolic stability. Also employed in research settings for the design of novel anti-inflammatory and anticancer agents.

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