4-Chloro-6-(methoxymethyl)-2-(pyridin-3-yl)pyrimidine

95%

Reagent Code: #156509
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CAS Number 339279-00-4

science Other reagents with same CAS 339279-00-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 235.67 g/mol
Formula C₁₁H₁₀ClN₃O
badge Registry Numbers
MDL Number MFCD00794779
thermostat Physical Properties
Boiling Point 276 °C
inventory_2 Storage & Handling
Density 1.27 g/cm3
Storage 2-8°C, light-proof, inert gas

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of kinase inhibitors for targeted cancer therapies. Its structure enables selective binding to specific enzyme active sites, making it valuable in drug discovery programs focused on oncology. It is also employed in the preparation of agrochemicals, where it contributes to the activity of certain herbicides and plant growth regulators. Due to its reactive sites, it serves as a building block in organic synthesis, facilitating the construction of complex heterocyclic systems in medicinal chemistry research.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿6,250.00
inventory 250mg
10-20 days ฿11,100.00
inventory 1g
10-20 days ฿29,980.00

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4-Chloro-6-(methoxymethyl)-2-(pyridin-3-yl)pyrimidine
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Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of kinase inhibitors for targeted cancer therapies. Its structure enables selective binding to specific enzyme active sites, making it valuable in drug discovery programs focused on oncology. It is also employed in the preparation of agrochemicals, where it contributes to the activity of certain herbicides and plant growth regulators. Due to its reactive sites, it serves as a building block in organic sy

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of kinase inhibitors for targeted cancer therapies. Its structure enables selective binding to specific enzyme active sites, making it valuable in drug discovery programs focused on oncology. It is also employed in the preparation of agrochemicals, where it contributes to the activity of certain herbicides and plant growth regulators. Due to its reactive sites, it serves as a building block in organic synthesis, facilitating the construction of complex heterocyclic systems in medicinal chemistry research.

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