6-chloro-5-methoxypyridine-3-carbonitrile

≥95%

Reagent Code: #159261
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CAS Number 1256835-79-6

science Other reagents with same CAS 1256835-79-6

blur_circular Chemical Specifications

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Weight 168.58 g/mol
Formula C₇H₅ClN₂O
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MDL Number MFCD18071080
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Storage Room temperature

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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other biologically active compounds. Its structure supports the formation of nitrogen-containing heterocycles, which are common in drugs targeting inflammation, cancer, and central nervous system disorders. The nitrile and chloro functional groups allow for further chemical modifications, making it valuable in medicinal chemistry for building complex molecules through cross-coupling, nucleophilic substitution, or cyclization reactions. It is also employed in agrochemical research for designing new pesticides and herbicides due to its reactivity and stability in synthetic pathways.

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inventory 1g
10-20 days ฿12,740.00

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6-chloro-5-methoxypyridine-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 biologically active compounds. Its structure supports the formation of nitrogen-containing heterocycles, which are common in drugs targeting inflammation, cancer, and central nervous system disorders. The nitrile and chloro functional groups allow for further chemical modifications, making it valuable in medicinal chemistry for building complex molecules through cross-coupling, n

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other biologically active compounds. Its structure supports the formation of nitrogen-containing heterocycles, which are common in drugs targeting inflammation, cancer, and central nervous system disorders. The nitrile and chloro functional groups allow for further chemical modifications, making it valuable in medicinal chemistry for building complex molecules through cross-coupling, nucleophilic substitution, or cyclization reactions. It is also employed in agrochemical research for designing new pesticides and herbicides due to its reactivity and stability in synthetic pathways.

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