86455-96-1 Usage
Chemical structure
A complex structure consisting of a xanthene ring with a hydroxyl group and a methyl group attached, and an aminoethylamino group, which is a derivative of dimethylaminoethylamine.
Molecular weight
327.38 g/mol
Functional groups
Xanthene ring, hydroxyl group, methyl group, amino group, and dimethylaminoethyl group.
Appearance
Yellow crystalline solid
Solubility
Soluble in organic solvents such as dimethyl sulfoxide (DMSO), methanol, and ethanol.
Fluorescent dye
Used in various applications due to its unique structure and properties.
Fluorescent label
Useful for labeling and tracking biomolecules like proteins and nucleic acids in biological and medical research.
Fluorescence microscopy
Employed to visualize and analyze cellular structures and processes.
Flow cytometry
Utilized for the analysis of cell populations based on the fluorescence properties of the labeled biomolecules.
Stability
Relatively stable under normal laboratory conditions, but sensitive to light and should be protected from exposure.
Safety
Handle with care, as it may have potential hazards depending on its concentration and exposure. Follow proper safety protocols and guidelines for its use.
Synonyms
Some common synonyms for 1-{[2-(dimethylamino)ethyl]amino}-7-hydroxy-4-methyl-9H-xanthen-9-one include DMAE-X, Xanthene dye, and 7-hydroxy-4-methyl-9-[2-(dimethylamino)ethylamino]-9H-xanthen-9-one.
Check Digit Verification of cas no
The CAS Registry Mumber 86455-96-1 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 6 respectively.
Calculate Digit Verification of CAS Registry Number 86455-96:
(7*8)+(6*6)+(5*4)+(4*5)+(3*5)+(2*9)+(1*6)=171
171 % 10 = 1
So 86455-96-1 is a valid CAS Registry Number.
86455-96-1Relevant academic research and scientific papers
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.
