2-sulfanylnicotinonitrile

≥95%

Reagent Code: #237581
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CAS Number 52505-45-0

science Other reagents with same CAS 52505-45-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 136.18 g/mol
Formula C₆H₄N₂S
badge Registry Numbers
MDL Number MFCD07343855
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of antiviral and anticancer agents. Its structure supports the formation of biologically active heterocyclic compounds. Commonly employed in medicinal chemistry for constructing pyridine-based scaffolds that enhance drug binding and selectivity. Also utilized in agrochemicals for designing novel pesticides due to its reactivity and ability to form stable derivatives. Serves as a ligand in catalytic systems for cross-coupling reactions, improving efficiency in organic synthesis.

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inventory 5g
10-20 days ฿12,010.00

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2-sulfanylnicotinonitrile
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of antiviral and anticancer agents. Its structure supports the formation of biologically active heterocyclic compounds. Commonly employed in medicinal chemistry for constructing pyridine-based scaffolds that enhance drug binding and selectivity. Also utilized in agrochemicals for designing novel pesticides due to its reactivity and ability to form stable derivatives. Serves as a ligand in catalytic systems for

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of antiviral and anticancer agents. Its structure supports the formation of biologically active heterocyclic compounds. Commonly employed in medicinal chemistry for constructing pyridine-based scaffolds that enhance drug binding and selectivity. Also utilized in agrochemicals for designing novel pesticides due to its reactivity and ability to form stable derivatives. Serves as a ligand in catalytic systems for cross-coupling reactions, improving efficiency in organic synthesis.

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