3-((Pyridin-4-ylmethyl)amino)propanenitrile

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Reagent Code: #228255
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CAS Number 648409-30-7

science Other reagents with same CAS 648409-30-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 161.2 g/mol
Formula C₉H₁₁N₃
badge Registry Numbers
MDL Number MFCD00121809
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 ability to participate in ring-forming reactions and form biologically active molecules. Its nitrile and amine functional groups allow for further chemical modifications, making it valuable in medicinal chemistry for optimizing drug potency and selectivity. Also employed in research settings for designing novel compounds with potential neurological or anti-inflammatory activity.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿17,120.00
inventory 5g
10-20 days ฿51,350.00

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3-((Pyridin-4-ylmethyl)amino)propanenitrile
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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 ability to participate in ring-forming reactions and form biologically active molecules. Its nitrile and amine functional groups allow for further chemical modifications, making it valuable in medicinal chemistry for optimizing drug potency and selectivity. Also emp

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 ability to participate in ring-forming reactions and form biologically active molecules. Its nitrile and amine functional groups allow for further chemical modifications, making it valuable in medicinal chemistry for optimizing drug potency and selectivity. Also employed in research settings for designing novel compounds with potential neurological or anti-inflammatory activity.

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