2-Methyl-5-bromopyrimidine-4-carboxylic acid

≥95%

Reagent Code: #208795
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CAS Number 100707-39-9

science Other reagents with same CAS 100707-39-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 217.02 g/mol
Formula C₆H₅BrN₂O₂
badge Registry Numbers
MDL Number MFCD00466678
thermostat Physical Properties
Boiling Point 335.2°C at 760 mmHg
inventory_2 Storage & Handling
Storage Room temperature, dry seal

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 creating drug candidates for cancer therapy and antiviral treatments. Commonly employed in cross-coupling reactions such as Suzuki-Miyaura, enabling the formation of carbon-carbon bonds in complex molecules. Also utilized in agrochemical research for designing novel pesticides and herbicides due to its ability to modulate biological activity in target organisms.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,050.00
inventory 250mg
10-20 days ฿1,630.00
inventory 1g
10-20 days ฿3,280.00
inventory 10g
10-20 days ฿26,560.00
inventory 5g
10-20 days ฿15,230.00
2-Methyl-5-bromopyrimidine-4-carboxylic acid
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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 creating drug candidates for cancer therapy and antiviral treatments. Commonly employed in cross-coupling reactions such as Suzuki-Miyaura, enabling the formation of carbon-carbon bonds in complex molecules. Also utilized in agrochemical research for designing novel pesticid

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 creating drug candidates for cancer therapy and antiviral treatments. Commonly employed in cross-coupling reactions such as Suzuki-Miyaura, enabling the formation of carbon-carbon bonds in complex molecules. Also utilized in agrochemical research for designing novel pesticides and herbicides due to its ability to modulate biological activity in target organisms.

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