6-(Chloromethyl)-N,N-dimethylpyridin-2-amine

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Reagent Code: #72594
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CAS Number 405103-62-0

science Other reagents with same CAS 405103-62-0

blur_circular Chemical Specifications

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Weight 170.64 g/mol
Formula C₈H₁₁ClN₂
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

6-(Chloromethyl)-N,N-dimethylpyridin-2-amine is primarily utilized in organic synthesis as a versatile intermediate. Its structure, featuring a chloromethyl group, makes it a valuable building block for constructing more complex molecules, particularly in the development of pharmaceuticals and agrochemicals. The compound is often employed in nucleophilic substitution reactions, where the chloromethyl group can be easily replaced by other functional groups, enabling the creation of diverse derivatives. Additionally, it is used in the synthesis of pyridine-based compounds, which are significant in medicinal chemistry due to their biological activity. The presence of the dimethylamino group further enhances its reactivity, allowing for modifications that can lead to the development of compounds with potential therapeutic applications.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿4,347.00
inventory 250mg
10-20 days ฿13,086.00

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6-(Chloromethyl)-N,N-dimethylpyridin-2-amine
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6-(Chloromethyl)-N,N-dimethylpyridin-2-amine is primarily utilized in organic synthesis as a versatile intermediate. Its structure, featuring a chloromethyl group, makes it a valuable building block for constructing more complex molecules, particularly in the development of pharmaceuticals and agrochemicals. The compound is often employed in nucleophilic substitution reactions, where the chloromethyl group can be easily replaced by other functional groups, enabling the creation of diverse derivatives. Ad

6-(Chloromethyl)-N,N-dimethylpyridin-2-amine is primarily utilized in organic synthesis as a versatile intermediate. Its structure, featuring a chloromethyl group, makes it a valuable building block for constructing more complex molecules, particularly in the development of pharmaceuticals and agrochemicals. The compound is often employed in nucleophilic substitution reactions, where the chloromethyl group can be easily replaced by other functional groups, enabling the creation of diverse derivatives. Additionally, it is used in the synthesis of pyridine-based compounds, which are significant in medicinal chemistry due to their biological activity. The presence of the dimethylamino group further enhances its reactivity, allowing for modifications that can lead to the development of compounds with potential therapeutic applications.

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