86455-97-2 Usage
Molecular structure
A complex chemical compound with a xanthene ring as its core structure.
Xanthene ring
A central part of the molecule, consisting of a fused six-membered and five-membered ring system.
Hydroxy group
A hydroxyl (-OH) group is present at position 7 of the xanthene ring.
Hydroxymethyl group
A hydroxymethyl (-CH2OH) group is attached at position 4 of the xanthene ring.
Aminoethylamine moiety
An amino group (-NH2) connected to an ethylamine chain is attached at position 1 of the xanthene ring.
Diethylamino substituent
The ethylamine chain in the aminoethylamine moiety has two additional ethyl groups (-CH2CH3) attached to the nitrogen atom.
Potential applications
The compound has possible uses in medicinal chemistry, fluorescent dyes, and biological imaging.
Unique structure
The combination of the xanthene ring, hydroxy groups, and the diethylamino-substituted aminoethylamine moiety provides a distinctive structure.
Functional groups
The presence of hydroxy, hydroxymethyl, and diethylamino groups contribute to the compound's properties and potential applications.
Research and development
The compound's structure and functional groups make it an interesting subject for further study in organic chemistry and pharmaceuticals.
Check Digit Verification of cas no
The CAS Registry Mumber 86455-97-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,4,5 and 5 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 86455-97:
(7*8)+(6*6)+(5*4)+(4*5)+(3*5)+(2*9)+(1*7)=172
172 % 10 = 2
So 86455-97-2 is a valid CAS Registry Number.
86455-97-2Relevant academic research and scientific papers
7-Hydroxylucanthone, 7-hydroxhycanthone and their analogs
-
, (2008/06/13)
7-Hydroxylucanthone and 7-hydroxyhycanthone derivatives have been found to have significant antitumor effect. The derivatives are of the general formula: STR1 wherein the radicals R1 and R2 are lower alkyl groups or other simple groups and R3 is OH where X=O, and H or OH where X=S.
Analogues of hycanthone and lucanthone as antitumor agents
Archer,Zayed,Rej,Rugino
, p. 1240 - 1246 (2007/10/02)
Hycanthone analogues (5 and 6) containing 7-substituted hydroxyl groups were prepared and evaluated as antitumor agents. These compounds were significantly more active than the corresponding unsubtituted derivatives. The 7-hydroxylated-4-(hydroxymethyl)-9H-xanthen-9-ones, 11 and 12, were also active antitumor agents. However, the 7-hydroxy-9H-xanthen-9-one counterparts of the 7-hydroxylucanthones were totally devoid of antitumor activity. Results obtained thus far are consistent with the hypothesis that 4-hydroxymethyl substituents in the 9H-xanthen-9-one and 9H-thioxanthen-9-one series are required for antitumor activity.
