2-Bromo-5-methylpyrimidine

98%

Reagent Code: #145133
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CAS Number 150010-20-1

science Other reagents with same CAS 150010-20-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 173.01 g/mol
Formula C₅H₅BrN₂
thermostat Physical Properties
Boiling Point 265°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and antiviral agents. Its structure, featuring a bromine at the activated 2-position of the pyrimidine ring, enables selective nucleophilic aromatic substitution (SNAr) and cross-coupling reactions, making it valuable in medicinal chemistry for constructing complex heterocyclic systems. Commonly employed in cross-coupling reactions such as Suzuki and Negishi couplings to form carbon-carbon bonds in drug discovery pipelines. Also utilized in agrochemical research for designing new active ingredients in crop protection products.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿720.00
inventory 1g
10-20 days ฿2,240.00
inventory 5g
10-20 days ฿10,990.00
inventory 25g
10-20 days ฿46,480.00

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2-Bromo-5-methylpyrimidine
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and antiviral agents. Its structure, featuring a bromine at the activated 2-position of the pyrimidine ring, enables selective nucleophilic aromatic substitution (SNAr) and cross-coupling reactions, making it valuable in medicinal chemistry for constructing complex heterocyclic systems. Commonly employed in cross-coupling reactions such as Suzuki and Negishi couplings to form carbon-carbon

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and antiviral agents. Its structure, featuring a bromine at the activated 2-position of the pyrimidine ring, enables selective nucleophilic aromatic substitution (SNAr) and cross-coupling reactions, making it valuable in medicinal chemistry for constructing complex heterocyclic systems. Commonly employed in cross-coupling reactions such as Suzuki and Negishi couplings to form carbon-carbon bonds in drug discovery pipelines. Also utilized in agrochemical research for designing new active ingredients in crop protection products.

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