4-Bromo-N,N-dimethylthiazol-2-amine

98%

Reagent Code: #215808
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CAS Number 209260-76-4

science Other reagents with same CAS 209260-76-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 207.09 g/mol
Formula C₅H₇BrN₂S
badge Registry Numbers
MDL Number MFCD09878986
inventory_2 Storage & Handling
Storage 2-8°C, Sealed, Inert Gas

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other biologically active compounds. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for creating drug candidates targeting cancer and inflammatory diseases. Also employed in agrochemical research for designing novel pesticides and herbicides due to its ability to enhance molecular binding and stability. Commonly utilized in Suzuki and Buchwald-Hartwig coupling reactions to build complex heterocyclic systems in both academic and industrial settings.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿6,030.00
250mg
10-20 days ฿10,240.00
4-Bromo-N,N-dimethylthiazol-2-amine
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other biologically active compounds. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for creating drug candidates targeting cancer and inflammatory diseases. Also employed in agrochemical research for designing novel pesticides and herbicides due to its ability to enhance molecular binding and stability. Commonly utilized in Suzuki and Bu

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other biologically active compounds. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for creating drug candidates targeting cancer and inflammatory diseases. Also employed in agrochemical research for designing novel pesticides and herbicides due to its ability to enhance molecular binding and stability. Commonly utilized in Suzuki and Buchwald-Hartwig coupling reactions to build complex heterocyclic systems in both academic and industrial settings.

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