(4-methoxypyridin-2-yl)methanamine dihydrochloride

≥95%

Reagent Code: #205648
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CAS Number 1344046-06-5

science Other reagents with same CAS 1344046-06-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 211.09 g/mol
Formula C₇H₁₂Cl₂N₂O
badge Registry Numbers
MDL Number MFCD20327973
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a key 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 amine functionality and pyridine core, which are common motifs in bioactive molecules. Its methoxy-substituted pyridine structure enhances binding selectivity in drug-receptor interactions. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies and optimization of drug candidates targeting inflammatory and oncological diseases.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿360.00
inventory 500mg
10-20 days ฿1,280.00
inventory 1g
10-20 days ฿1,930.00
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(4-methoxypyridin-2-yl)methanamine dihydrochloride
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Used as a key 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 amine functionality and pyridine core, which are common motifs in bioactive molecules. Its methoxy-substituted pyridine structure enhances binding selectivity in drug-receptor interactions. Commonly employed in medicinal chemistry for structure-activity rel

Used as a key 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 amine functionality and pyridine core, which are common motifs in bioactive molecules. Its methoxy-substituted pyridine structure enhances binding selectivity in drug-receptor interactions. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies and optimization of drug candidates targeting inflammatory and oncological diseases.

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