4-Chloro-N-methylpyridine-2-carboxamide

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Reagent Code: #159018
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CAS Number 220000-87-3

science Other reagents with same CAS 220000-87-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 170.6 g/mol
Formula C₇H₇ClN₂O
badge Registry Numbers
MDL Number MFCD02185921
thermostat Physical Properties
Melting Point 41-43°C
inventory_2 Storage & Handling
Storage -20°C

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 medicinal chemistry due to its ability to form stable heterocyclic structures that interact with biological targets. Commonly employed in the preparation of small-molecule drugs targeting inflammatory diseases and neurological disorders. Its chloro and carboxamide functional groups allow for further chemical modifications, making it valuable in structure-activity relationship studies during drug discovery. Also utilized in agrochemical research for designing new pesticides with improved selectivity and efficacy.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿156.00
inventory 5g
10-20 days ฿320.00
inventory 25g
10-20 days ฿900.00
inventory 100g
10-20 days ฿2,860.00
inventory 500g
10-20 days ฿13,360.00

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4-Chloro-N-methylpyridine-2-carboxamide
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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 medicinal chemistry due to its ability to form stable heterocyclic structures that interact with biological targets. Commonly employed in the preparation of small-molecule drugs targeting inflammatory diseases and neurological disorders. Its chloro and carboxamide functional groups allow for further chemical modifications, making it va

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 medicinal chemistry due to its ability to form stable heterocyclic structures that interact with biological targets. Commonly employed in the preparation of small-molecule drugs targeting inflammatory diseases and neurological disorders. Its chloro and carboxamide functional groups allow for further chemical modifications, making it valuable in structure-activity relationship studies during drug discovery. Also utilized in agrochemical research for designing new pesticides with improved selectivity and efficacy.

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