Tris(4-bromophenyl)phosphane

95%

Reagent Code: #68869
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CAS Number 29949-81-3

science Other reagents with same CAS 29949-81-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 498.97 g/mol
Formula C₁₈H₁₂Br₃P
badge Registry Numbers
MDL Number MFCD02690473
inventory_2 Storage & Handling
Storage room temperature, inert gas storage

description Product Description

Used as a ligand in coordination chemistry to stabilize metal complexes, particularly in catalytic reactions. It is employed in cross-coupling reactions, such as Suzuki-Miyaura and Heck reactions, to facilitate the formation of carbon-carbon bonds. Its electron-rich nature enhances the efficiency of palladium and other transition metal catalysts. Additionally, it finds application in organic synthesis for constructing complex molecular architectures, including pharmaceuticals and fine chemicals. Its brominated aromatic groups contribute to its stability and reactivity in various chemical transformations.

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Test Parameter Specification
Appearance White to yellow powder or crystals
Purity 94.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿4,490.00
inventory 250mg
10-20 days ฿1,970.00
inventory 100mg
10-20 days ฿1,170.00

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Tris(4-bromophenyl)phosphane
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Used as a ligand in coordination chemistry to stabilize metal complexes, particularly in catalytic reactions. It is employed in cross-coupling reactions, such as Suzuki-Miyaura and Heck reactions, to facilitate the formation of carbon-carbon bonds. Its electron-rich nature enhances the efficiency of palladium and other transition metal catalysts. Additionally, it finds application in organic synthesis for constructing complex molecular architectures, including pharmaceuticals and fine chemicals. Its brom

Used as a ligand in coordination chemistry to stabilize metal complexes, particularly in catalytic reactions. It is employed in cross-coupling reactions, such as Suzuki-Miyaura and Heck reactions, to facilitate the formation of carbon-carbon bonds. Its electron-rich nature enhances the efficiency of palladium and other transition metal catalysts. Additionally, it finds application in organic synthesis for constructing complex molecular architectures, including pharmaceuticals and fine chemicals. Its brominated aromatic groups contribute to its stability and reactivity in various chemical transformations.

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