(4-Methylpyridin-3-yl)methanamine

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Reagent Code: #210362
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CAS Number 1443-42-1

science Other reagents with same CAS 1443-42-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 122.17 g/mol
Formula C₇H₁₀N₂
badge Registry Numbers
MDL Number MFCD06213859
thermostat Physical Properties
Boiling Point 242.8 °C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other bioactive molecules. Its structure allows for easy functionalization, making it valuable in medicinal chemistry for creating compounds with potential anti-inflammatory, anticancer, or neuroprotective activities. Also employed in the preparation of agrochemicals and specialty chemicals due to its nitrogen-containing heterocyclic scaffold. Commonly utilized in research settings for building more complex molecules through coupling reactions or condensation processes.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿3,490.00
inventory 1g
10-20 days ฿10,100.00
inventory 5g
10-20 days ฿43,610.00

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(4-Methylpyridin-3-yl)methanamine
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other bioactive molecules. Its structure allows for easy functionalization, making it valuable in medicinal chemistry for creating compounds with potential anti-inflammatory, anticancer, or neuroprotective activities. Also employed in the preparation of agrochemicals and specialty chemicals due to its nitrogen-containing heterocyclic scaffold. Commonly utilized in research settings for

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other bioactive molecules. Its structure allows for easy functionalization, making it valuable in medicinal chemistry for creating compounds with potential anti-inflammatory, anticancer, or neuroprotective activities. Also employed in the preparation of agrochemicals and specialty chemicals due to its nitrogen-containing heterocyclic scaffold. Commonly utilized in research settings for building more complex molecules through coupling reactions or condensation processes.

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