1213-82-7 Usage
Chemical Family
Anthracene compounds
Structural Features
Presence of a chloro group and a cyano group on the 10th and 9th positions of the anthracene molecule
Usage
Building block for the synthesis of various organic compounds
Applications
Pharmaceutical, dyes, and fluorescent materials
Intermediate
Preparation of complex organic molecules
Photophysical Properties
Useful for materials science and optoelectronics
Versatility
Unique structural features make it a valuable intermediate
Organic Chemistry
Commonly used in the field of organic chemistry
Synthesis
Used for the synthesis of various organic compounds
Molecular Structure
Characterized by the presence of a chloro and cyano group on specific positions of the anthracene molecule
Check Digit Verification of cas no
The CAS Registry Mumber 1213-82-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,2,1 and 3 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1213-82:
(6*1)+(5*2)+(4*1)+(3*3)+(2*8)+(1*2)=47
47 % 10 = 7
So 1213-82-7 is a valid CAS Registry Number.
InChI:InChI=1/C15H8ClN/c16-15-12-7-3-1-5-10(12)14(9-17)11-6-2-4-8-13(11)15/h1-8H
1213-82-7Relevant articles and documents
The Reaction of Iodine Monochloride with Polycyclic Aromatic Compounds: Polar and Electron Transfer Pathways
Turner, Dean E.,O'Malley, Robert F.,Sardella, Dennis J.,Barinelli, Lucio S.,Kaul, Pushkar
, p. 7335 - 7340 (1994)
Several polycyclic aromatic hydrocarbons were treated with iodine monochloride.Although iodination is the predominant reaction of benzenoid arenes, chlorination is the sole reaction with anthracene, phenanthrene and naphthalene compounds (except for 5), whose oxidation half-wave potentials are less than 1.58 V vs Ag/Ag(+) (0.1 M).Arenes with higher potentials are unreactive.Naphthalene (9) and its derivatives with mild electron-withdrawing substituents are chlorinated; the exception (5) yields the 1-iodo product (21).The reaction is first order in substrate and second order in ICl.An electron transfer pathway involving radical cation intermediates is assumed.Ion-pair collapse of the radical cation-ICl intermediates is proposed for the chlorinations and radical-pair collapse for the iodination.
Synthese von Zimtsaeurenitrilen und 9-Chlor-10-cyano-anthracen durch modifizierte Vilsmeier-Haack-Arnold-Reaktion
Liebscher, Juergen,Bechstein, Ute
, p. 56 - 57 (2007/10/02)
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