(4-Bromophenyl)dimesitylborane

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Reagent Code: #154599
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CAS Number 38186-40-2

science Other reagents with same CAS 38186-40-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 405.18 g/mol
Formula C₂₄H₂₆BBr
badge Registry Numbers
MDL Number MFCD31731346
inventory_2 Storage & Handling
Storage Room temperature, seal, dry, inert gas

description Product Description

Used as a key intermediate in organic synthesis, particularly in the preparation of boron-containing conjugated materials for optoelectronic applications. It serves as a building block in the development of organic light-emitting diodes (OLEDs) and sensors due to its electron-deficient boron center and stable arylborane structure. The compound is also employed in Suzuki-Miyaura cross-coupling reactions to construct complex aromatic systems. Its steric bulk from mesityl groups enhances stability and influences regioselectivity in catalytic reactions. Additionally, it finds use in the study of charge-transfer complexes and luminescent materials.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿6,940.00
inventory 250mg
10-20 days ฿11,770.00
inventory 1g
10-20 days ฿38,950.00

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(4-Bromophenyl)dimesitylborane
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Used as a key intermediate in organic synthesis, particularly in the preparation of boron-containing conjugated materials for optoelectronic applications. It serves as a building block in the development of organic light-emitting diodes (OLEDs) and sensors due to its electron-deficient boron center and stable arylborane structure. The compound is also employed in Suzuki-Miyaura cross-coupling reactions to construct complex aromatic systems. Its steric bulk from mesityl groups enhances stability and influ

Used as a key intermediate in organic synthesis, particularly in the preparation of boron-containing conjugated materials for optoelectronic applications. It serves as a building block in the development of organic light-emitting diodes (OLEDs) and sensors due to its electron-deficient boron center and stable arylborane structure. The compound is also employed in Suzuki-Miyaura cross-coupling reactions to construct complex aromatic systems. Its steric bulk from mesityl groups enhances stability and influences regioselectivity in catalytic reactions. Additionally, it finds use in the study of charge-transfer complexes and luminescent materials.

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