916180-10-4 Usage
Methyl ester derivative
1H-Indole-4-carboxylic acid This indicates that the compound is derived from 1H-Indole-4-carboxylic acid and has a methyl ester group attached.
Carboxylic acid group
Functional group This indicates that the compound contains a carboxylic acid group, which is a common functional group in organic chemistry.
Iodine atom
Attached to third position of indole ring This indicates that the compound contains an iodine atom attached to the third position of the indole ring, which can affect its chemical properties and reactivity.
Used in pharmaceutical research and drug development
Potential biological activity and therapeutic applications This indicates that the compound has potential for use in pharmaceutical research and drug development due to its biological activity and potential therapeutic applications.
Valuable building block
Synthesis of various organic compounds This indicates that the compound can be used as a building block in the synthesis of other organic compounds, making it a valuable reagent in organic chemistry.
Employed in chemical and biochemical studies
Reagent and precursor This indicates that the compound is used as a reagent and precursor in chemical and biochemical studies, allowing for the preparation of other functionalized molecules.
Check Digit Verification of cas no
The CAS Registry Mumber 916180-10-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,6,1,8 and 0 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 916180-10:
(8*9)+(7*1)+(6*6)+(5*1)+(4*8)+(3*0)+(2*1)+(1*0)=154
154 % 10 = 4
So 916180-10-4 is a valid CAS Registry Number.
916180-10-4Relevant academic research and scientific papers
Construction of Cyclopenta[b]indol-1-ones by a Tandem Gold(I)-Catalyzed Rearrangement/Nazarov Reaction and Application to the Synthesis of Bruceolline H
Scarpi, Dina,Petrovi?, Martina,Fiser, Béla,Gómez-Bengoa, Enrique,Occhiato, Ernesto G.
supporting information, p. 3922 - 3925 (2016/08/16)
A tandem gold(I)-catalyzed rearrangement/Nazarov reaction of enynyl acetates which efficiently provides cyclopenta[b]indol-1-ones as useful precursors for the synthesis of natural and bioactive compounds is described. The synthetic potential of the method
TREATMENT OF PROTEIN FOLDING DISORDERS
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Page/Page column 107, (2010/11/25)
In certain embodiments, the invention is directed to a method for treating a protein folding disorder such as Alzheimer's disease, dementia, Parkinson's disease, Huntington's disease and prion-based spongiform encephalopathy. The method comprises the administration to a subject of a compound of the formula (I) wherein A and B are independently a mono- or bicyclic aromatic group or heteroaromatic cyclic group. In preferred embodiments, the compounds are bis-indole compounds.
