6407-59-6 Usage
Chemical class
1-hydrazinoanthraquinone belongs to the class of anthraquinone derivatives, which are commonly used as dyes and pigments.
Appearance
It is a yellowish-orange crystalline powder.
Solubility
1-hydrazinoanthraquinone is soluble in organic solvents.
Potential applications
It has been extensively studied for its potential applications in organic and material chemistry, particularly as a precursor for the synthesis of functionalized anthraquinone derivatives.
Reactivity
Its unique properties and reactivity make it a valuable building block for the preparation of various organic compounds.
Importance in manufacturing
1-hydrazinoanthraquinone is an important intermediate in the manufacturing of dyes and pigments.
Potential use in pharmaceuticals
Studies have shown its potential use in chemical reactions for the production of pharmaceuticals and other organic compounds.
Check Digit Verification of cas no
The CAS Registry Mumber 6407-59-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,4,0 and 7 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 6407-59:
(6*6)+(5*4)+(4*0)+(3*7)+(2*5)+(1*9)=96
96 % 10 = 6
So 6407-59-6 is a valid CAS Registry Number.
InChI:InChI=1/C14H10N2O2/c15-16-11-7-3-6-10-12(11)14(18)9-5-2-1-4-8(9)13(10)17/h1-7,16H,15H2
6407-59-6Relevant articles and documents
EDC-mediated condensations of 1-chloro-5-hydrazino-9,10-anthracenedione, 1-hydrazino-9,10-anthracenedione, and the corresponding anthrapyrazoles
Kim, MeeKyoung,Wiemer, David F.
, p. 4977 - 4980 (2007/10/03)
The EDC-mediated condensation of 1-chloro-5-hydrazino-9,10-anthracenedione afforded an N-1 acyl anthrapyrazole instead of the expected hydrazide. The regiochemistry of the N-acyl substituent was assigned on the basis of an extensive set of NMR experiments, and identification of this isomer suggests a reaction sequence based on initial acylation and subsequent cyclization. In contrast, the parallel reaction of 1-hydrazino-9,10-anthracenedione proceeded to afford the expected hydrazide.
Tripeptide probes for tripeptidyl protease I production via gene transfer
Kim, MeeKyoung,Mao, Qinwen,Davidson, Beverly L.,Wiemer, David F.
, p. 1603 - 1608 (2007/10/03)
Tripeptides derived from 5-chloroanthraquinone hydrazide and anthraquinone hydrazide have been prepared as potential reagents to probe cellular expression of tripeptidyl protease I (TPP-I). Attempted chemical synthesis of Gly-L-Pro-L-Ala-chloroanthraquino
