1210-12-4 | 9-Anthracenecarbonitrile

Packsize	Purity	Availability	Price	Discounted Price
1g	95%	in stock	$23.00	$16.00
5g	95%	in stock	$78.00	$54.00
25g	95%	in stock	$239.00	$167.00
100g	95%	in stock	$789.00	$552.00

Description

• Catalog Number: AB70303
• Chemical Name: 9-Anthracenecarbonitrile
• CAS Number: 1210-12-4
• Molecular Formula: C15H9N
• Molecular Weight: 203.2387
• MDL Number: MFCD00001242
• SMILES: N#Cc1c2ccccc2cc2c1cccc2
• NSC Number: 26997

Computed Properties

• Complexity: 278
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 16
• Hydrogen Bond Acceptor Count: 1
• XLogP3: 4.3

Upstream Synthesis Route

$Name$ is a versatile compound commonly used in chemical synthesis due to its unique properties and reactivity. In particular, 9-Anthracenecarbonitrile serves as a valuable building block in the creation of various organic compounds and materials.One key application of 9-Anthracenecarbonitrile is its role as a precursor in the synthesis of anthracene derivatives, which are widely employed in the production of dyes, pigments, and fluorescent materials. By undergoing various chemical reactions such as nucleophilic substitution or transition metal-catalyzed transformations, 9-Anthracenecarbonitrile can be transformed into functionalized anthracene compounds with tailored properties.Additionally, 9-Anthracenecarbonitrile can also be utilized in the preparation of heterocyclic compounds, pharmaceutical intermediates, and organic electronic materials. Its ability to undergo diverse synthetic pathways makes it a valuable tool for organic chemists and material scientists seeking to develop novel molecules with specific functionalities.Overall, the versatility and reactivity of 9-Anthracenecarbonitrile make it an indispensable compound in chemical synthesis, offering endless possibilities for the creation of advanced materials and compounds in various fields of research and industry.

Literature

• Probing the interplay between factors determining reaction rates on silica gel using termolecular systems.

  Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology 20121001

• Investigations on the photoreactions of phenothiazine and phenoxazine in presence of 9-cyanoanthracene by using steady state and time resolved spectroscopic techniques.

  Journal of fluorescence 20100901

• Photophysics of aromatic thiourea derivatives and their complexes with anions. Fast and ultrafast spectroscopic investigations.

  Physical chemistry chemical physics : PCCP 20100728

• High-throughput acousto-optic-tunable-filter-based time-resolved fluorescence spectrometer for optical biopsy.

  Optics letters 20090401

• Unexpectedly similar charge transfer rates through benzo-annulated bicyclo[2.2.2]octanes.

  Journal of the American Chemical Society 20080618

• Effects of liquid crystal environment on the spectroscopic and photophysical properties of well-known reacting systems 2,3-dimethylindole (DMI) and 9-cyanoanthracene (9CNA).

  The journal of physical chemistry. A 20071115

• Fluorescence lifetime standards for time and frequency domain fluorescence spectroscopy.

  Analytical chemistry 20070301

• Emission from charge recombination during the pulse radiolysis of arylethynylpyrenes.

  The journal of physical chemistry. B 20060706

• Asymmetric photocycloaddition in solution of a chiral crystallized naphthamide.

  Angewandte Chemie (International ed. in English) 20050826

• Efficient emission from charge recombination during the pulse radiolysis of electrochemical luminescent donor-acceptor molecules with an ethynyl linkage.

  The Journal of organic chemistry 20050819

• Pendular-state spectroscopy of the S(1)-S(0) electronic transition of 9-cyanoanthracene.

  The Journal of chemical physics 20041115

• Primary electron-transfer dynamics in 2-phenylindole-9-cyanoanthracene system. A comparative study with 2-methylindole.

  Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy 20040701

• Marcus theory of outer-sphere heterogeneous electron transfer reactions: dependence of the standard electrochemical rate constant on the hydrodynamic radius from high precision measurements of the oxidation of anthracene and its derivatives in nonaqueous solvents using the high-speed channel electrode.

  Journal of the American Chemical Society 20040519

• Non-radiative depletion of the excited electronic states of 9-cyanoanthracene in presence of tetrahydronaphthols.

  Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy 20030201

• The use of nonpolar matrices for matrix-assisted laser desorption/ionization mass spectrometric analysis of high boiling crude oil fractions.

  Rapid communications in mass spectrometry : RCM 20030101

• Chemoenzymatic synthesis and properties of Schiff bases containing (R)-1-(9-anthryl)ethylamine.

  Chirality 20020801

• Nature of non-radiative processes involved in the excited state of 9-cyanoanthracene in presence of 2-methylindole/2-methylindoline quenchers. A laser flash photolysis study to reveal the medium effects.

  Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy 20020601

• Synthesis and studies on spectroscopic as well as electron donating properties of the two alkoxy benzo[b]thiophenes.

  Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy 20011201