23060-42-6 Usage
Chemical structure
1-amino-4-[(4-methoxyphenyl)amino]anthraquinone
Type of compound
Synthetic compound
Usage
Red dye in the textile industry
Derivative of
Anthraquinone
Contains
Amino group and a 4-methoxyphenyl group
Known for
Bright and intense red color
Potential applications
Organic electronics, fluorescent probe for detecting metal ions
Safety concerns
Harmful if ingested or inhaled, may cause skin and eye irritation upon contact
Precautions
Handle with care
Check Digit Verification of cas no
The CAS Registry Mumber 23060-42-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,0,6 and 0 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 23060-42:
(7*2)+(6*3)+(5*0)+(4*6)+(3*0)+(2*4)+(1*2)=66
66 % 10 = 6
So 23060-42-6 is a valid CAS Registry Number.
InChI:InChI=1/C21H16N2O3/c1-26-13-8-6-12(7-9-13)23-17-11-10-16(22)18-19(17)21(25)15-5-3-2-4-14(15)20(18)24/h2-11,23H,22H2,1H3
23060-42-6Relevant articles and documents
Arylamination of Aminohalogenoanthraquinones
Philip, George,Nabar, U. T.,Kanetkar, V. R.,Sunthankar, S. V.
, p. 808 - 811 (2007/10/02)
1-Amino-4-arylaminoanthraquinones (II) have been prepared in high yields by reacting 1-amino-4-chloroanthraquinone (Ia, 1 mol) with arylamines (6 mol) and anhyd.AlCl3 (5 mol) in nitrobenzene at room temperature. 1-Amino-2-bromoanthraquinone, 2-amino-1-chloroanthraquinone, 1-benzamido-4-chloroanthraquinone and 1-amino-5-chloroanthraquinone fail to give arylaminated products. 1-Amino-2,4-dibromoanthraquinone (Ic) gives only 4-arylaminated compounds (IIq-s) whereas 1-amino-8-chloroanthraquinone (Ie) gives 2-arylaminated derivatives (III).A plausible mechanism for the reaction has been suggested.The arylaminated compounds have been applied on polyester as disperse dyes and their dyeing properties evaluated.
