4-Methoxy-2-oxo-1,2-dihydro-pyridine-3-carbonitrile

95%

Reagent Code: #205843
label
Alias 3-Cyano-2-hydroxy-4-methoxypyrimidine; 4-methoxy-3-cyano-2(1H)-pyridone; 2-oxo-4-methoxy-1,2-dihydropyridine-3-carbonitrile; Gimoster Intermediate Di; 4-methoxy-2-oxo-1,2-dihydropyridine-3-cyanoformitrile
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CAS Number 21642-98-8

science Other reagents with same CAS 21642-98-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 150.13 g/mol
Formula C₇H₆N₂O₂
badge Registry Numbers
MDL Number MFCD00975442
thermostat Physical Properties
Melting Point 293 °C
Boiling Point 421.8 °C at 760 mmHg
inventory_2 Storage & Handling
Density 1.27±0.1 g/cm3(Predicted)
Storage Room temperature, inert gas

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 supports the formation of heterocyclic compounds with potential antitumor, antiviral, and anti-inflammatory activities. Commonly employed in medicinal chemistry for scaffold modification to enhance drug potency and selectivity. Also utilized in agrochemical research for designing new pesticides and herbicides due to its reactivity and ability to form stable derivatives.

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Size Availability Unit Price Quantity
inventory 100g
10-20 days ฿2,370.00
4-Methoxy-2-oxo-1,2-dihydro-pyridine-3-carbonitrile
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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 supports the formation of heterocyclic compounds with potential antitumor, antiviral, and anti-inflammatory activities. Commonly employed in medicinal chemistry for scaffold modification to enhance drug potency and selectivity. Also utilized in agrochemical research for designing new pesticides and herbicides due to its reactivity and ability to

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other bioactive molecules. Its structure supports the formation of heterocyclic compounds with potential antitumor, antiviral, and anti-inflammatory activities. Commonly employed in medicinal chemistry for scaffold modification to enhance drug potency and selectivity. Also utilized in agrochemical research for designing new pesticides and herbicides due to its reactivity and ability to form stable derivatives.

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