4,6-Dibromo-1,2-dihydroisoquinolin-1-one

95%

Reagent Code: #178157
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CAS Number 1254514-08-3

science Other reagents with same CAS 1254514-08-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 302.95 g/mol
Formula C₉H₅Br₂NO
badge Registry Numbers
MDL Number MFCD18426476
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and central nervous system (CNS) active compounds. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for building bioactive molecules. It is also employed in research settings to design compounds with potential antitumor, anti-inflammatory, and neuroprotective properties. The compound’s bromine substituents enable cross-coupling reactions, facilitating the creation of diverse chemical libraries for drug discovery.

Available Sizes & Pricing

Size Availability Unit Price Quantity
50mg
10-20 days ฿1,830.00
100mg
10-20 days ฿2,870.00
250mg
10-20 days ฿5,600.00
4,6-Dibromo-1,2-dihydroisoquinolin-1-one
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and central nervous system (CNS) active compounds. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for building bioactive molecules. It is also employed in research settings to design compounds with potential antitumor, anti-inflammatory, and neuroprotective properties. The compound’s bromine substituents enable cross-coupling reactions, faci

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and central nervous system (CNS) active compounds. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for building bioactive molecules. It is also employed in research settings to design compounds with potential antitumor, anti-inflammatory, and neuroprotective properties. The compound’s bromine substituents enable cross-coupling reactions, facilitating the creation of diverse chemical libraries for drug discovery.

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