5-Iodo-2-methylthiazole

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Reagent Code: #200807
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CAS Number 1412902-50-1

science Other reagents with same CAS 1412902-50-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 225.05 g/mol
Formula C₄H₄INS
badge Registry Numbers
MDL Number MFCD22479546
inventory_2 Storage & Handling
Storage 2-8°C, light-proof, inert gas

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of antiviral and anticancer agents. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for building complex heterocyclic compounds. Commonly employed in cross-coupling reactions like Suzuki and Heck reactions to form carbon-carbon bonds in drug discovery pipelines. Also utilized in agrochemical research for designing bioactive molecules with enhanced stability and reactivity.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿8,280.00
inventory 250mg
10-20 days ฿14,080.00
inventory 5g
10-20 days ฿52,730.00
inventory 1g
10-20 days ฿36,540.00

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5-Iodo-2-methylthiazole
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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 allows for selective functionalization, making it valuable in medicinal chemistry for building complex heterocyclic compounds. Commonly employed in cross-coupling reactions like Suzuki and Heck reactions to form carbon-carbon bonds in drug discovery pipelines. Also utilized in agrochemical research for designing bioactive molecules with enhanced stability and r

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of antiviral and anticancer agents. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for building complex heterocyclic compounds. Commonly employed in cross-coupling reactions like Suzuki and Heck reactions to form carbon-carbon bonds in drug discovery pipelines. Also utilized in agrochemical research for designing bioactive molecules with enhanced stability and reactivity.

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