2-Chloro-4-(3-methoxyphenyl)pyrimidine

95%

Reagent Code: #156864
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CAS Number 499195-50-5

science Other reagents with same CAS 499195-50-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 220.655 g/mol
Formula C₁₁H₉ClN₂O
badge Registry Numbers
MDL Number MFCD09800977
inventory_2 Storage & Handling
Storage 2-8°C, Inert Gas

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in the preparation of active pharmaceutical ingredients (APIs) due to its reactive chloro and aryl groups, which allow for further functionalization through cross-coupling reactions. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies to optimize drug candidates targeting inflammatory diseases and oncology. Also utilized in agrochemical research for designing novel pesticides with improved efficacy and selectivity.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿2,970.00
inventory 1g
10-20 days ฿7,990.00
inventory 5g
10-20 days ฿27,920.00

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2-Chloro-4-(3-methoxyphenyl)pyrimidine
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in the preparation of active pharmaceutical ingredients (APIs) due to its reactive chloro and aryl groups, which allow for further functionalization through cross-coupling reactions. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies to optimize drug candidates targeting inflammatory diseases and oncol

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in the preparation of active pharmaceutical ingredients (APIs) due to its reactive chloro and aryl groups, which allow for further functionalization through cross-coupling reactions. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies to optimize drug candidates targeting inflammatory diseases and oncology. Also utilized in agrochemical research for designing novel pesticides with improved efficacy and selectivity.

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