2606-86-2 Usage
Chemical structure
A derivative of anthracene, a polycyclic aromatic hydrocarbon, with a chlorine atom and an amino group attached to the core.
Functional groups
Amino group (-NH2) and carbonyl group (C=O) present in the molecule.
Appearance
The compound may appear as a solid or crystalline material.
Applications
Used in the production of dyes, pigments, and organic synthesis.
Biological activities
Potential anti-cancer agent.
Hazards
May pose hazards to human health and the environment.
Handling precautions
Should be handled and used with caution due to potential hazards.
Check Digit Verification of cas no
The CAS Registry Mumber 2606-86-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,6,0 and 6 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 2606-86:
(6*2)+(5*6)+(4*0)+(3*6)+(2*8)+(1*6)=82
82 % 10 = 2
So 2606-86-2 is a valid CAS Registry Number.
2606-86-2Relevant articles and documents
The Schmidt reaction of anthraquinones
Flemming, Cecily A.,Gandhi, Sham S.,Gibson, Martin S.,Ruediger, Edward H.
, p. 624 - 628 (2007/10/02)
Schmidt reaction (sodium azide/sulfuric acid) of 1,5- and of 1,8-dichloroanthraquinones gives, in each case, both of the theoretically possible lactams (2,3,5,6-dibenzoazepin-4,7-diones).Two of the four theoretically possible lactams have been identified from Schmidt reaction of 1- and 2-chloroanthraquinones respectively.Methods used include:(a) preferential hydrolysis of one lactam and identification of the isomeric aminoanthraquinone formed on cyclodehydration of the resulting amino acid; (b) identification of the isomeric aminoanthraquinone(s) formed on direct treatment of a lactam (or mixture of lactams) by sulfuric acid; (c) cleavage by potassium tert-butoxide of the amino acid formed by preferential hydrolysis of one lactam and identification of the resulting benzoic acid as its methyl ester.
