Methyl 2-iodobenzoate

98%

Reagent Code: #204700
label
Alias 2-iodobenzoate; methyl orthoiodobenzoate, methyl 2-iodobenzoate
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CAS Number 610-97-9

science Other reagents with same CAS 610-97-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 262.04 g/mol
Formula C₈H₇IO₂
badge Registry Numbers
EC Number 210-243-6
MDL Number MFCD00016351
thermostat Physical Properties
Boiling Point 149-150 °C/10 mm Hg(lit.)
inventory_2 Storage & Handling
Density 1.784 g/mL at 25 °C(lit.)
Storage Room temperature, avoid light

description Product Description

Used as an intermediate in organic synthesis, particularly in pharmaceutical and agrochemical manufacturing. It serves as a building block in the preparation of heterocyclic compounds and bioactive molecules. Commonly employed in cross-coupling reactions, such as Suzuki and Heck reactions, due to the presence of the iodine atom, which facilitates metal-catalyzed transformations. Also utilized in the development of dyes, fragrances, and functional materials where aromatic ester derivatives are required.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 10g
10-20 days ฿280.00
inventory 50g
10-20 days ฿720.00
inventory 250g
10-20 days ฿2,590.00
inventory 1kg
10-20 days ฿8,930.00

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Methyl 2-iodobenzoate
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Used as an intermediate in organic synthesis, particularly in pharmaceutical and agrochemical manufacturing. It serves as a building block in the preparation of heterocyclic compounds and bioactive molecules. Commonly employed in cross-coupling reactions, such as Suzuki and Heck reactions, due to the presence of the iodine atom, which facilitates metal-catalyzed transformations. Also utilized in the development of dyes, fragrances, and functional materials where aromatic ester derivatives are required.

Used as an intermediate in organic synthesis, particularly in pharmaceutical and agrochemical manufacturing. It serves as a building block in the preparation of heterocyclic compounds and bioactive molecules. Commonly employed in cross-coupling reactions, such as Suzuki and Heck reactions, due to the presence of the iodine atom, which facilitates metal-catalyzed transformations. Also utilized in the development of dyes, fragrances, and functional materials where aromatic ester derivatives are required.

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