1055-23-8 | 9,9'-Bianthracene

Packsize	Purity	Availability	Price	Discounted Price
250mg	95%	in stock	$60.00	$42.00
1g	95%	in stock	$73.00	$51.00
5g	95%	in stock	$162.00	$113.00
10g	95%	in stock	$308.00	$216.00
25g	95%	in stock	$660.00	$462.00

Description

• Catalog Number: AD68287
• Chemical Name: 9,9'-Bianthracene
• CAS Number: 1055-23-8
• Molecular Formula: C28H18
• Molecular Weight: 354.4425
• MDL Number: MFCD00130216
• SMILES: c1ccc2c(c1)c(c1c(c2)cccc1)c1c2ccccc2cc2c1cccc2
• NSC Number: 179353

Computed Properties

• Complexity: 444
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 28
• Rotatable Bond Count: 1
• XLogP3: 8.5

Upstream Synthesis Route

9,9'-Bianthracene, a versatile organic compound, is widely utilized in chemical synthesis as a powerful building block in the creation of various advanced materials. Its unique structure and reactivity make it an essential component in the development of organic light-emitting diodes (OLEDs), organic semiconductors, and other optoelectronic devices. Furthermore, 9,9'-Bianthracene serves as a valuable precursor in the synthesis of functionalized anthracene derivatives, which have applications in medicinal chemistry, materials science, and organic synthesis. Its exceptional photochemical and photophysical properties make it a crucial intermediate in the production of innovative materials with tailored properties for a range of industrial and scientific applications.

Literature

• Analysis of the solvatochromism of 9,9'-biaryl compounds using a pure solvent dipolarity scale.

  The journal of physical chemistry. A 20120517

• Two different charge transfer states of photoexcited 9,9'-bianthryl in polar and nonpolar solvents characterized by nanosecond time-resolved near-IR spectroscopy in the 4500-10,500 cm(-1) region.

  The journal of physical chemistry. A 20100610

• Femtosecond time-resolved absorption anisotropy spectroscopy on 9,9'-bianthryl: detection of partial intramolecular charge transfer in polar and nonpolar solvents.

  The Journal of chemical physics 20090107

• Ultrafast charge transfer process of 9,9'-bianthryl in imidazolium ionic liquids.

  The journal of physical chemistry. B 20081211

• Charge resonance character in the charge transfer state of bianthryls: effect of symmetry breaking on time-resolved near-IR absorption spectra.

  The journal of physical chemistry. A 20060406

• QM/MM study of the role of the solvent in the formation of the charge separated excited state in 9,9'-bianthryl.

  Journal of the American Chemical Society 20050810

• Isolation of axial conformers of chloro- and bromocyclohexane in a pure state as inclusion complexes with 9,9'-bianthryl, and the discovery of a novel 1,3 diaxial Cl...H weak interaction.

  Chemical communications (Cambridge, England) 20050807

• Highly conjugated p-quinonoid pi-extended tetrathiafulvalene derivatives: a class of highly distorted electron donors.

  Chemistry (Weinheim an der Bergstrasse, Germany) 20040419

• Symmetry breaking in the relaxed S(1) excited state of bianthryl derivatives in weakly polar solvents.

  Journal of the American Chemical Society 20010606