4392-73-8 Usage
Explanation
10-iminoanthracen-9(10H)-one is composed of 15 carbon atoms, 9 hydrogen atoms, 1 nitrogen atom, and 1 oxygen atom.
Explanation
10-iminoanthracen-9(10H)-one is derived from anthracene, a polycyclic aromatic hydrocarbon, by attaching a nitrogen atom to the 10th position of the anthracene ring.
Explanation
The nitrogen atom in 10-iminoanthracen-9(10H)-one is attached to the 10th position of the anthracene ring, which differentiates it from other iminoanthracene derivatives.
Explanation
10-iminoanthracen-9(10H)-one is used as a fluorescent dye in biological and medical research due to its ability to emit light when exposed to specific wavelengths of light.
Explanation
This compound is used in organic synthesis for the production of other complex compounds, taking advantage of its unique chemical properties.
Explanation
Due to its unique chemical and structural properties, 10-iminoanthracen-9(10H)-one has potential uses in the development of new materials and pharmaceuticals.
Explanation
It is important to handle 10-iminoanthracen-9(10H)-one with care, as it may have potential risks and hazards associated with its use, such as toxicity or reactivity with other substances.
Explanation
The anthracene ring in 10-iminoanthracen-9(10H)-one is planar, and the compound has an extended conjugated system, which contributes to its unique chemical and optical properties.
Explanation
10-iminoanthracen-9(10H)-one is relatively stable under normal conditions, but it can still react with other chemicals, especially under specific conditions or in the presence of certain reagents.
Explanation
This compound is generally soluble in organic solvents, such as ethanol, methanol, and dimethyl sulfoxide (DMSO), which facilitates its use in various applications and experiments.
Derivative of anthracene
Yes
Nitrogen atom position
10th position
Fluorescent dye
Yes
Organic synthesis
Yes
Potential applications
Development of new materials and pharmaceuticals
Handling precautions
Careful handling required
Chemical structure
Planar and conjugated
Stability
Relatively stable
Solubility
Soluble in organic solvents
Check Digit Verification of cas no
The CAS Registry Mumber 4392-73-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,3,9 and 2 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 4392-73:
(6*4)+(5*3)+(4*9)+(3*2)+(2*7)+(1*3)=98
98 % 10 = 8
So 4392-73-8 is a valid CAS Registry Number.
4392-73-8Relevant articles and documents
Rose Bengal Functionalized Phase-Transfer Catalysts Promoting Photooxidations with Singlet Oxygen. Nucleophilic Displacements on Dioxetanic and Endoperoxidic Intermediates
Guarini, Alessandro,Tundo, Pietro
, p. 3501 - 3508 (2007/10/02)
Photooxidations with 1O2 promoted by an anionic photosensitizer, such as Rose Bengal, can be readily performed in an aqueous-organic, two-phase system in the presence of catalytic amounts of quaternary onium salts that transfer the anion in the organic phase, This means that one can use low-polar solvents, which are unusual in reactions with this sensitizer.Soluble and silica gel immobilized onium salts were used as the phase-transfer catalysts.If a nucleophile is also present in the reaction mixture, it, too, is transported in the organic phase and reacts via SN2, if the intermediate is of the dioxetanic or endoperoxidic type.With the heterogenized catalysts it is possible to carry out the reaction in two steps: the photooxidation itself and later the nucleophilic displacement.In addition to being productive with regard to the synthesis, this can clarify the photooxidation reaction pathway.The following organic substrates were photooxidized under PTC conditions: anthracene, 2,3-dimethyl-2-butene, 5,6-dihydro-2,3-diphenyl-p-dioxin, 1,3-cyclohexadiene, and indene.In the presence of N3- as nucleophile, anthracene gives 10-imino-9(10H)-anthracenone while 5,6-dihydro-2,3-diphenyl-p-dioxin yields, selectively, two different azido derivatives according to the procedure employed.
