1-tert-butyl-3-iodobenzene

95%

Reagent Code: #242243
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CAS Number 58164-02-6

science Other reagents with same CAS 58164-02-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 260.12 g/mol
Formula C₁₀H₁₃I
thermostat Physical Properties
Boiling Point 244.6ºC at 760mmHg
inventory_2 Storage & Handling
Density 1.459g/cm3
Storage Room temperature

description Product Description

Used primarily as a building block in organic synthesis, especially in cross-coupling reactions such as Suzuki and Heck reactions. Its iodo functionality allows for efficient metal-catalyzed bond formation, making it valuable in the preparation of pharmaceuticals, agrochemicals, and functional materials. The tert-butyl group acts as a sterically bulky substituent, which can influence regioselectivity and stability in reaction pathways. Commonly employed in the development of liquid crystals and advanced intermediates where controlled substitution patterns are required.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿930.00
inventory 1g
10-20 days ฿2,070.00
inventory 5g
10-20 days ฿6,140.00
inventory 25g
10-20 days ฿21,390.00

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1-tert-butyl-3-iodobenzene
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Used primarily as a building block in organic synthesis, especially in cross-coupling reactions such as Suzuki and Heck reactions. Its iodo functionality allows for efficient metal-catalyzed bond formation, making it valuable in the preparation of pharmaceuticals, agrochemicals, and functional materials. The tert-butyl group acts as a sterically bulky substituent, which can influence regioselectivity and stability in reaction pathways. Commonly employed in the development of liquid crystals and advanced

Used primarily as a building block in organic synthesis, especially in cross-coupling reactions such as Suzuki and Heck reactions. Its iodo functionality allows for efficient metal-catalyzed bond formation, making it valuable in the preparation of pharmaceuticals, agrochemicals, and functional materials. The tert-butyl group acts as a sterically bulky substituent, which can influence regioselectivity and stability in reaction pathways. Commonly employed in the development of liquid crystals and advanced intermediates where controlled substitution patterns are required.

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