86456-18-0 Usage
Uses
Used in Dye Chemistry:
1-[2-(dimethylamino)ethyl]amino-7-hydroxy-9H-xanthen-9-one is used as a fluorescent dye due to its unique molecular structure and potential to emit light upon excitation, making it suitable for applications in imaging and detection technologies.
Used in Medicinal Chemistry:
As a pharmaceutical intermediate, 1-[2-(dimethylamino)ethyl]amino-7-hydroxy-9H-xanthen-9-one may be utilized in the development of new drugs, given its complex structure that could interact with biological targets in innovative ways.
Used in Material Science:
1-[2-(dimethylamino)ethyl]amino-7-hydroxy-9H-xanthen-9-one is used as a chemical probe in biological research, allowing scientists to study its interactions with various biological systems and potentially leading to advancements in understanding cellular processes and mechanisms.
Due to the unique structure and potential of 1-[2-(dimethylamino)ethyl]amino-7-hydroxy-9H-xanthen-9-one, further exploration of its properties and applications is necessary to fully harness its capabilities in these fields.
Check Digit Verification of cas no
The CAS Registry Mumber 86456-18-0 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 6 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 86456-18:
(7*8)+(6*6)+(5*4)+(4*5)+(3*6)+(2*1)+(1*8)=160
160 % 10 = 0
So 86456-18-0 is a valid CAS Registry Number.
86456-18-0Relevant academic research and scientific papers
7-Hydroxylucanthone, 7-hydroxhycanthone and their analogs
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, (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.
