2,6-Dichloropyridine-3,5-Dicarbonitrile

97%

Reagent Code: #179020
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CAS Number 151229-84-4

science Other reagents with same CAS 151229-84-4

blur_circular Chemical Specifications

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Weight 198.01 g/mol
Formula C₇HCl₂N₃
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the production of nicotinic acetylcholine receptor modulators. It serves as a building block in agrochemicals for developing herbicides and insecticides due to its stable aromatic structure and reactive nitrile groups. Also employed in the manufacture of dyes and functional materials where nitrogen-rich heterocycles enhance electronic properties. Its chloro and cyano functionalities allow for selective cross-coupling reactions, making it valuable in research and development of novel organic compounds.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿6,050.00
inventory 250mg
10-20 days ฿9,040.00
inventory 1g
10-20 days ฿22,580.00
inventory 5g
10-20 days ฿71,480.00

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2,6-Dichloropyridine-3,5-Dicarbonitrile
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the production of nicotinic acetylcholine receptor modulators. It serves as a building block in agrochemicals for developing herbicides and insecticides due to its stable aromatic structure and reactive nitrile groups. Also employed in the manufacture of dyes and functional materials where nitrogen-rich heterocycles enhance electronic properties. Its chloro and cyano functionalities allow for selective cross-coupling reaction

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the production of nicotinic acetylcholine receptor modulators. It serves as a building block in agrochemicals for developing herbicides and insecticides due to its stable aromatic structure and reactive nitrile groups. Also employed in the manufacture of dyes and functional materials where nitrogen-rich heterocycles enhance electronic properties. Its chloro and cyano functionalities allow for selective cross-coupling reactions, making it valuable in research and development of novel organic compounds.

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