2-Iodoresorcinol

97%(GC)

Reagent Code: #200007
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CAS Number 41046-67-7

science Other reagents with same CAS 41046-67-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 236.01 g/mol
Formula C₆H₅IO₂
badge Registry Numbers
MDL Number MFCD09701440
thermostat Physical Properties
Melting Point 108°C
inventory_2 Storage & Handling
Storage -20°C, inert gas

description Product Description

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. Its structure allows for selective functionalization, making it valuable in the development of complex molecules. Commonly employed in coupling reactions, such as Suzuki or Heck reactions, due to the presence of the iodine atom, which facilitates cross-coupling processes. Also utilized in the synthesis of dyes and fluorescent compounds owing to its phenolic nature and substitution pattern.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,080.00
inventory 1g
10-20 days ฿2,410.00
inventory 5g
10-20 days ฿8,450.00
inventory 25g
10-20 days ฿25,650.00

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2-Iodoresorcinol
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Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. Its structure allows for selective functionalization, making it valuable in the development of complex molecules. Commonly employed in coupling reactions, such as Suzuki or Heck reactions, due to the presence of the iodine atom, which facilitates cross-coupling processes. Also utilized in the synthesis of dyes and fluorescent compounds owing to its phenolic nature and substitution pattern.<

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. Its structure allows for selective functionalization, making it valuable in the development of complex molecules. Commonly employed in coupling reactions, such as Suzuki or Heck reactions, due to the presence of the iodine atom, which facilitates cross-coupling processes. Also utilized in the synthesis of dyes and fluorescent compounds owing to its phenolic nature and substitution pattern.

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