2-Ethynyl-4-nitropyridine

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Reagent Code: #55310
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CAS Number 1211515-78-4

science Other reagents with same CAS 1211515-78-4

blur_circular Chemical Specifications

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Weight 148.1189 g/mol
Formula C₇H₄N₂O₂
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Storage room temperature

description Product Description

Used primarily in organic synthesis, this compound serves as a key intermediate in the development of pharmaceuticals and agrochemicals. Its structure, featuring both an ethynyl group and a nitro group, makes it valuable for constructing complex molecules through reactions like Sonogashira coupling and nucleophilic substitution. It is particularly useful in the synthesis of heterocyclic compounds, which are often found in drugs targeting various diseases. Additionally, its nitro group can be reduced to an amine, enabling further functionalization for creating bioactive molecules. In research, it is employed to study reaction mechanisms and develop new synthetic methodologies.

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inventory 50mg
10-20 days ฿6,012.00

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2-Ethynyl-4-nitropyridine
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Used primarily in organic synthesis, this compound serves as a key intermediate in the development of pharmaceuticals and agrochemicals. Its structure, featuring both an ethynyl group and a nitro group, makes it valuable for constructing complex molecules through reactions like Sonogashira coupling and nucleophilic substitution. It is particularly useful in the synthesis of heterocyclic compounds, which are often found in drugs targeting various diseases. Additionally, its nitro group can be reduced to a

Used primarily in organic synthesis, this compound serves as a key intermediate in the development of pharmaceuticals and agrochemicals. Its structure, featuring both an ethynyl group and a nitro group, makes it valuable for constructing complex molecules through reactions like Sonogashira coupling and nucleophilic substitution. It is particularly useful in the synthesis of heterocyclic compounds, which are often found in drugs targeting various diseases. Additionally, its nitro group can be reduced to an amine, enabling further functionalization for creating bioactive molecules. In research, it is employed to study reaction mechanisms and develop new synthetic methodologies.

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