5-Bromo-2-methoxy-4-methylpyrimidine

98%

Reagent Code: #146684
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CAS Number 38696-23-0

science Other reagents with same CAS 38696-23-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 203.04 g/mol
Formula C₆H₇BrN₂O
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 other biologically active compounds. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for building complex molecules. Commonly employed in cross-coupling reactions such as Suzuki or Negishi couplings to form carbon-carbon bonds in drug discovery programs. Also utilized in agrochemical research for designing new active ingredients in crop protection agents. Its bromine moiety facilitates easy substitution, enabling rapid diversification in library synthesis for high-throughput screening.

Available Sizes & Pricing

Size Availability Unit Price Quantity
25mg
10-20 days ฿990.00
100mg
10-20 days ฿2,280.00
1g
10-20 days ฿6,850.00
5g
10-20 days ฿27,460.00
5-Bromo-2-methoxy-4-methylpyrimidine
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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 building complex molecules. Commonly employed in cross-coupling reactions such as Suzuki or Negishi couplings to form carbon-carbon bonds in drug discovery programs. Also utilized in agrochemical research for designing new active ingredients in crop p

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 building complex molecules. Commonly employed in cross-coupling reactions such as Suzuki or Negishi couplings to form carbon-carbon bonds in drug discovery programs. Also utilized in agrochemical research for designing new active ingredients in crop protection agents. Its bromine moiety facilitates easy substitution, enabling rapid diversification in library synthesis for high-throughput screening.

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