1,3-Dibromo-5-(tert-butyl)benzene

95%

Reagent Code: #175826
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CAS Number 129316-09-2

science Other reagents with same CAS 129316-09-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 292.01 g/mol
Formula C₁₀H₁₂Br₂
badge Registry Numbers
MDL Number MFCD06657956
thermostat Physical Properties
Boiling Point 250°C at 760 mmHg
inventory_2 Storage & Handling
Storage Room temperature, dry seal

description Product Description

Used as an intermediate in organic synthesis, particularly in the preparation of functionalized aromatic compounds for pharmaceuticals and agrochemicals. It serves as a building block in cross-coupling reactions, such as Suzuki and Heck reactions, enabling the formation of carbon-carbon bonds. Its bromine substituents allow for selective substitution, making it valuable in the development of complex molecules in medicinal chemistry and materials science. Also employed in the synthesis of ligands and catalysts due to the stability imparted by the tert-butyl group.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿162.00
inventory 5g
10-20 days ฿690.00
inventory 10g
10-20 days ฿1,370.00
inventory 25g
10-20 days ฿3,410.00
inventory 100g
10-20 days ฿12,920.00

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1,3-Dibromo-5-(tert-butyl)benzene
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Used as an intermediate in organic synthesis, particularly in the preparation of functionalized aromatic compounds for pharmaceuticals and agrochemicals. It serves as a building block in cross-coupling reactions, such as Suzuki and Heck reactions, enabling the formation of carbon-carbon bonds. Its bromine substituents allow for selective substitution, making it valuable in the development of complex molecules in medicinal chemistry and materials science. Also employed in the synthesis of ligands and cata

Used as an intermediate in organic synthesis, particularly in the preparation of functionalized aromatic compounds for pharmaceuticals and agrochemicals. It serves as a building block in cross-coupling reactions, such as Suzuki and Heck reactions, enabling the formation of carbon-carbon bonds. Its bromine substituents allow for selective substitution, making it valuable in the development of complex molecules in medicinal chemistry and materials science. Also employed in the synthesis of ligands and catalysts due to the stability imparted by the tert-butyl group.

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