7511-49-1 | 1,3,5-Tris(4-bromophenyl)benzene

Packsize	Purity	Availability	Price	Discounted Price
1g	95%	in stock	$12.00	$8.00
5g	95%	in stock	$17.00	$12.00
10g	95%	in stock	$21.00	$15.00
25g	95%	in stock	$41.00	$29.00
100g	95%	in stock	$150.00	$105.00

Description

• Catalog Number: AB42650
• Chemical Name: 1,3,5-Tris(4-bromophenyl)benzene
• CAS Number: 7511-49-1
• Molecular Formula: C24H15Br3
• Molecular Weight: 543.0879
• MDL Number: MFCD00362911
• SMILES: Brc1ccc(cc1)c1cc(cc(c1)c1ccc(cc1)Br)c1ccc(cc1)Br
• NSC Number: 30660

Computed Properties

• Complexity: 364
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 27
• Rotatable Bond Count: 3
• XLogP3: 9.7

Upstream Synthesis Route

1,3,5-Tris(4-bromophenyl)benzene, also known as $name$, is a highly versatile compound widely utilized in chemical synthesis applications. This compound plays a crucial role in organic chemistry due to its unique structural properties and reactivity. As a tribrominated benzene derivative, $name$ is particularly valued for its ability to serve as a building block in the synthesis of various organic molecules.In chemical synthesis, 1,3,5-Tris(4-bromophenyl)benzene is commonly used as a key intermediate for the construction of complex organic compounds, such as dendrimers, polymers, and other functional materials. Its triphenylbenzene core offers a convenient platform for further functionalization through various chemical transformations, allowing for the introduction of different substituents or functional groups.The presence of three bromine atoms on the phenyl rings of $name$ also imparts unique reactivity to the molecule, making it a valuable precursor for cross-coupling reactions, halogenation processes, and other synthetic transformations. Additionally, the electron-withdrawing nature of the bromine substituents can influence the overall electronic properties of the molecule, leading to altered chemical behavior and enhanced reactivity in specific reactions.Overall, the strategic incorporation of 1,3,5-Tris(4-bromophenyl)benzene in chemical synthesis endeavors provides synthetic chemists with a versatile tool for designing and accessing novel organic compounds with tailored properties and functionalities.

Literature

• Dimerization of tri(4-bromophenyl)benzene by aryl-aryl coupling from solution on a gold surface.

  Journal of the American Chemical Society 20110330

• Microporous coordination polymers as selective sorbents for liquid chromatography.

  Langmuir : the ACS journal of surfaces and colloids 20091020

• Surface mediated synthesis of 2D covalent organic frameworks: 1,3,5-tris(4-bromophenyl)benzene on graphite(001), Cu(111), and Ag(110).

  Chemical communications (Cambridge, England) 20090807