86455-98-3 Usage
Uses
Used in Research Applications:
1-((2-(diMethylaMino)ethyl)aMino)-7-hydroxy-4-(hydroxyMethyl)-9H-xanthen-9-one is used as a research compound for exploring its potential biological activities and properties. Its presence in the Xanthones class suggests that it may exhibit antimicrobial, anti-inflammatory, or anticancer effects, which could be of interest to researchers in the fields of medicine and pharmaceuticals.
Used in Chemical Synthesis:
1-((2-(diMethylaMino)ethyl)aMino)-7-hydroxy-4-(hydroxyMethyl)-9H-xanthen-9-one is used as an intermediate product in chemical synthesis. Its complex structure and functional groups may be utilized in the production of other compounds or materials, particularly in the pharmaceutical or chemical industries.
Used in Pharmaceutical Development:
Although not explicitly stated, the potential biological activity of 1-((2-(diMethylaMino)ethyl)aMino)-7-hydroxy-4-(hydroxyMethyl)-9H-xanthen-9-one suggests that it could be used in pharmaceutical development. Its antimicrobial, anti-inflammatory, or anticancer properties may be harnessed to create new drugs or treatments, pending further investigation and validation.
Check Digit Verification of cas no
The CAS Registry Mumber 86455-98-3 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 8 respectively.
Calculate Digit Verification of CAS Registry Number 86455-98:
(7*8)+(6*6)+(5*4)+(4*5)+(3*5)+(2*9)+(1*8)=173
173 % 10 = 3
So 86455-98-3 is a valid CAS Registry Number.
InChI:InChI=1/C18H20N2O4/c1-20(2)8-7-19-14-5-3-11(10-21)18-16(14)17(23)13-9-12(22)4-6-15(13)24-18/h3-6,9,19,21-22H,7-8,10H2,1-2H3
86455-98-3Relevant 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.
