82-27-9 Usage
General Description
2-Amino-1-chloroanthraquinone is a chemical compound with the molecular formula C14H8ClNO2. It is a derivative of anthraquinone, which is commonly used in the production of dyes and pigments. 2-Amino-1-chloroanthraquinone is used in the manufacture of vat dyes, which are water-insoluble pigments that are particularly effective for coloring textiles. The compound has a chlorine atom and an amino group attached to the anthraquinone core, which gives it unique properties for dyeing applications. It has a dark red-brown color and is known for its high color fastness and resistance to fading, making it a popular choice for dyeing fabrics and other materials. Additionally, the compound has been studied for its potential use in organic synthesis and as a pharmaceutical intermediate.
Check Digit Verification of cas no
The CAS Registry Mumber 82-27-9 includes 5 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 2 digits, 8 and 2 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 82-27:
(4*8)+(3*2)+(2*2)+(1*7)=49
49 % 10 = 9
So 82-27-9 is a valid CAS Registry Number.
InChI:InChI=1/C14H8ClNO2/c15-12-10(16)6-5-9-11(12)14(18)8-4-2-1-3-7(8)13(9)17/h1-6H,16H2
82-27-9Relevant articles and documents
PHOTOCHEMICAL REACTION OF 9,10-ANTHRAQUINONE AND ITS DERIVATIVES WITH PYRIDINE
Loskutov, V.A.,Lukonina, S.M.,Konstantinova, A.V.,Fokin, E.P.
, p. 500 - 504 (2007/10/02)
The previously unknown photochemical reaction of 9,10-anthraquinone with pyridine in an atmosphere of argon takes place with formation of 2-(1,2-dihydropyridino)- or 2-(1,4-dihydropyridino)-9,10-anthraquinone, which is converted by the action of alkali into 2-aminoanthraquinone.In the presence of atmospheric oxygen the reaction product after treatment whith alkali is 1-aminoanthraquinone in addition to 2-aminoanthraquinone.The 1- and 2-methoxyanthraquinones and chloroanthraquinones react with pyridine in the light and form, after treatment with alkali, substituted aminoanthraquinones.