Cyanomethyl methyl(4-pyridyl)carbamodithioate

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Reagent Code: #162719
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CAS Number 1158958-89-4

science Other reagents with same CAS 1158958-89-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 223.32 g/mol
Formula C₉H₉N₃S₂
badge Registry Numbers
MDL Number MFCD23704391
thermostat Physical Properties
Melting Point 129-132°C &_& 3652-3697°C (lit.)
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other bioactive molecules targeting cancer and inflammatory diseases. Its structure allows for efficient derivatization, making it valuable in medicinal chemistry for constructing heterocyclic systems. Also employed in agrochemical research for designing novel pesticides with improved selectivity and potency. The compound's reactivity supports its role in forming carbon-sulfur and carbon-nitrogen bonds during multistep organic syntheses.

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inventory 1g
10-20 days ฿10,890.00

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Cyanomethyl methyl(4-pyridyl)carbamodithioate
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Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other bioactive molecules targeting cancer and inflammatory diseases. Its structure allows for efficient derivatization, making it valuable in medicinal chemistry for constructing heterocyclic systems. Also employed in agrochemical research for designing novel pesticides with improved selectivity and potency. The compound's reactivity supports its role in forming carbon-sulfur

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other bioactive molecules targeting cancer and inflammatory diseases. Its structure allows for efficient derivatization, making it valuable in medicinal chemistry for constructing heterocyclic systems. Also employed in agrochemical research for designing novel pesticides with improved selectivity and potency. The compound's reactivity supports its role in forming carbon-sulfur and carbon-nitrogen bonds during multistep organic syntheses.

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