86455-90-5 Usage
Chemical structure
A complex chemical compound with a thioxanthene backbone, a hydroxy and hydroxymethyl group attached, and an aminoethylamine side chain with a diethylamino group.
Molecular weight
Approximately 399.54 g/mol
Thioxanthene backbone
Aromatic ring system with a sulfur atom in the center.
Hydroxy group (-OH)
A polar functional group that can form hydrogen bonds.
Hydroxymethyl group (-CH2OH)
A functional group containing both hydroxy and methyl groups.
Amino group (-NH2)
A polar functional group that can form hydrogen bonds and coordinate with metal ions.
Diethylamino group (-N(C2H5)2)
A basic, lipophilic functional group with two ethyl substituents.
Pharmaceuticals
Due to its unique structure and properties, it may have potential uses in the development of new drugs.
Other industries
Its complex structure may also make it useful in other fields, such as materials science or chemical research.
Further research
Additional studies and analysis are needed to fully understand the compound's potential applications, effects, and interactions with other molecules.
Solubility
The compound's solubility in various solvents is not provided, but it can be inferred that it may be soluble in organic solvents due to the presence of lipophilic groups (e.g., diethylamino and hydroxymethyl groups).
Stability
Information on the compound's stability under different conditions is not provided, but its complex structure suggests that it may be sensitive to certain environmental factors, such as heat, light, or moisture.
Reactivity
The compound's reactivity with other molecules or functional groups is not provided, but its various functional groups (e.g., hydroxy, amino, and diethylamino) suggest that it may undergo various chemical reactions, such as hydrogen bonding, coordination, or substitution reactions.
Toxicity
Information on the compound's toxicity is not provided, but its complex structure and potential pharmaceutical applications suggest that its safety and potential side effects should be carefully evaluated.
Check Digit Verification of cas no
The CAS Registry Mumber 86455-90-5 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 0 respectively.
Calculate Digit Verification of CAS Registry Number 86455-90:
(7*8)+(6*6)+(5*4)+(4*5)+(3*5)+(2*9)+(1*0)=165
165 % 10 = 5
So 86455-90-5 is a valid CAS Registry Number.
86455-90-5Relevant 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.
