518-06-9 Usage
Chemical compound
1H-Indole,3,3',3''-methylidynetrisis a chemical compound, which means it is a substance composed of two or more elements chemically bonded together in a fixed ratio.
Derivative of indole
1H-Indole,3,3',3''-methylidynetrisis a derivative of indole, meaning that it is a compound that has been modified from the structure of the parent compound, indole, which is a heterocyclic aromatic organic compound.
Heterocyclic aromatic structure
The indole ring in 1H-Indole,3,3',3''-methylidynetrisis a heterocyclic aromatic structure, which means it contains a ring of atoms with at least one atom being a heteroatom (an atom other than carbon, such as nitrogen) and exhibits aromatic properties.
Three methylidynetriphenyl groups
1H-Indole,3,3',3''-methylidynetriscontains three methylidynetriphenyl groups attached to the indole ring, which are organic functional groups consisting of a carbon atom bonded to three phenyl groups (rings of six carbon atoms with alternating single and double bonds) and one methyl group (a carbon atom bonded to three hydrogen atoms).
Potential applications
1H-Indole,3,3',3''-methylidynetrismay have potential applications in chemical research and pharmaceutical development due to its unique structure and properties, such as its ability to interact with biological systems or serve as a building block for synthesizing other compounds.
Need for further research
Further research is needed to fully understand the potential uses and effects of 1H-Indole,3,3',3''-methylidynetris-, as its properties and applications may not yet be completely known or understood.
Check Digit Verification of cas no
The CAS Registry Mumber 518-06-9 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,1 and 8 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 518-06:
(5*5)+(4*1)+(3*8)+(2*0)+(1*6)=59
59 % 10 = 9
So 518-06-9 is a valid CAS Registry Number.
518-06-9Relevant articles and documents
Transformations of 3-formylindoles under the action of acids
Korolev,Yudina,Lazhko,Reznikova,Preobrazhenskaya
, p. 561 - 569 (2007/10/03)
Under the influence of acids 3-formylindole forms urorosein (the salt of di(indol-3-yl)methylium) which is unstable in solution and decomposes to give a series of indole derivatives, among which 6-(indol-3-yl)-5H,7H-indolo[2,3-b]carbazole and tri(indol-3-yl)methylium salt predominate. N,N′-Dimethylurorosein in solution also forms a mixture of indole derivatives, from which tri(1-methylindol-3-yl)methylium salt, 5N,11N-dimethylindolo[3,2-b]carbazole and its 6-(1-methylindol-3-yl) derivative were isolated. 1999 KluwerAcademic/Plenum Publishers.
Reactions of Ethyl 3-Ethoxymethylene-2,4-dioxovalerate and Ethyl Ethoxymethyleneoxaloacetate with Indole Analogs
Kurihara, Takushi,Tani, Tsutomu,Imai, Hiromi,Nasu, Keiko
, p. 2972 - 2979 (2007/10/02)
The reactions of ethyl 3-ethoxymethylene-2,4-dioxovalerate (1a) and ethyl ethoxymethyleneoxaloacetate (1b) with indole analogs (2, 14, 17-19) are described.Treatment of 1a, b with 2 in ethanol followed by refluxing in acetic anhydride afforded 3,4,10-trisubstituted pyrimidoindoles (4a, b).Hydrogenation or nucleophilic addition of 4a, b was found to occur on the pyrimidine ring in a 1,4-fashion.Compounds 1a, b were also reacted with 14 in ethanol under ice cooling to give the 3,4-disubstituted 9H-pyrimidoindoles (15a, b) directly.Indole (17) or 2-methylindole (18) reacted with 1a (or 1b) to give a mixture of 3-indolylmethylene derivatives (20a, b and 21a, b) and tris-(3-indolyl)-methanes (23 and 24).
