5-(Chloromethyl)nicotinonitrile hydrochloride

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Reagent Code: #81455
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CAS Number 189936-27-4

science Other reagents with same CAS 189936-27-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 189.04 g/mol
Formula C₇H₆Cl₂N₂
badge Registry Numbers
MDL Number MFCD28252259
inventory_2 Storage & Handling
Storage 2-8°C, store under inert gas

description Product Description

Used in pharmaceutical research, it serves as a key intermediate in the synthesis of various bioactive compounds, particularly those targeting neurological and cardiovascular diseases. Its structure is valuable in developing nicotinamide derivatives, which are explored for their potential therapeutic effects. Additionally, it is employed in organic synthesis to create complex molecules for drug discovery and development. Its reactive chloromethyl group allows for further functionalization, making it a versatile building block in medicinal chemistry.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,248.00
inventory 250mg
10-20 days ฿6,444.00
inventory 1g
10-20 days ฿19,341.00
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5-(Chloromethyl)nicotinonitrile hydrochloride
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Used in pharmaceutical research, it serves as a key intermediate in the synthesis of various bioactive compounds, particularly those targeting neurological and cardiovascular diseases. Its structure is valuable in developing nicotinamide derivatives, which are explored for their potential therapeutic effects. Additionally, it is employed in organic synthesis to create complex molecules for drug discovery and development. Its reactive chloromethyl group allows for further functionalization, making it a ve

Used in pharmaceutical research, it serves as a key intermediate in the synthesis of various bioactive compounds, particularly those targeting neurological and cardiovascular diseases. Its structure is valuable in developing nicotinamide derivatives, which are explored for their potential therapeutic effects. Additionally, it is employed in organic synthesis to create complex molecules for drug discovery and development. Its reactive chloromethyl group allows for further functionalization, making it a versatile building block in medicinal chemistry.

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