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.

Available Sizes & Pricing

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