2987-66-8 Usage
Type of compound
Derivative of anthraquinone
Usage
Dye in textile industry
Affinity
Strong for cellulose fibers
Popularity
Used for dyeing cotton and other cellulose-based materials
Additional uses
Production of colored paper, plastics, and other synthetic materials
Pharmaceutical applications
Fluorescent marker and in the development of certain drugs
Safety concerns
Hazardous effects on human health and the environment if not used and disposed of properly
Check Digit Verification of cas no
The CAS Registry Mumber 2987-66-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,9,8 and 7 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 2987-66:
(6*2)+(5*9)+(4*8)+(3*7)+(2*6)+(1*6)=128
128 % 10 = 8
So 2987-66-8 is a valid CAS Registry Number.
InChI:InChI=1/C16H14N2O2/c1-17-11-7-3-5-9-13(11)15(19)10-6-4-8-12(18-2)14(10)16(9)20/h3-8,17-18H,1-2H3
2987-66-8Relevant articles and documents
STRUCTURE OF THE BORATE COMPLEXES OF α-AMINO AND α-HYDROXY-9,10-ANTHRAQUINONES AND THEIR REACTION WITH AMINES
Gorelik, M. V.,Shapet'ko, N. N.,Arinich, L. V.,Tsurkan, A. I.,Kukushkina, M. L.
, p. 547 - 556 (2007/10/02)
It was shown by 13C NMR that a redistribution of the bonds with partial localization of the 1,5- and 1,10-anthraquinonoid structures occurs during the transition from 1,5-diamino(dihydroxy)- and 1-amino(hydroxy)-9,10-anthraquinones respectively to their borate complexes.For this reason the boroacetates and fluoroborates of 1,5-dihydroxyanthraquinonones, 1-aminoanthraquinones, their N-alkyl and N-aryl derivatives, and 1,5-dihydroxyanthraquinone are capable of entering into amination under the influence of aromatic amines with substitution of the hydrogen atom at position 4 under mild conditions with the participation of atmospheric oxygen as oxidizing agent