N,N-Diisopropylisonicotinamide

95%

Reagent Code: #219219
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CAS Number 77924-05-1

science Other reagents with same CAS 77924-05-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 206.28 g/mol
Formula C₁₂H₁₈N₂O
badge Registry Numbers
MDL Number MFCD00085693
thermostat Physical Properties
Boiling Point 327.8±15.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.007±0.06 g/cm3(Predicted)
Storage 2-8°C

description Product Description

Used as an intermediate in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. Its structure supports the formation of nitrogen-containing heterocyclic compounds, which are common in bioactive molecules. It also serves as a building block in the preparation of functionalized pyridine derivatives, useful in medicinal chemistry for drug discovery. Additionally, it can act as a ligand or reagent in catalytic reactions, aiding in the formation of carbon–carbon or carbon–heteroatom bonds.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,440.00
inventory 250mg
10-20 days ฿3,900.00
inventory 1g
10-20 days ฿10,540.00

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N,N-Diisopropylisonicotinamide
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Used as an intermediate in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. Its structure supports the formation of nitrogen-containing heterocyclic compounds, which are common in bioactive molecules. It also serves as a building block in the preparation of functionalized pyridine derivatives, useful in medicinal chemistry for drug discovery. Additionally, it can act as a ligand or reagent in catalytic reactions, aiding in the formation of carbon–carbon or carbon–h

Used as an intermediate in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. Its structure supports the formation of nitrogen-containing heterocyclic compounds, which are common in bioactive molecules. It also serves as a building block in the preparation of functionalized pyridine derivatives, useful in medicinal chemistry for drug discovery. Additionally, it can act as a ligand or reagent in catalytic reactions, aiding in the formation of carbon–carbon or carbon–heteroatom bonds.

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