441715-30-6 Usage
Description
5-FLUORO-1-METHYL-1H-INDOLE-3-CARBALDEHYDE is a chemical compound with the molecular formula C10H8FNO. It is a fluorescent yellow solid that is commonly used in organic synthesis and medicinal chemistry. 5-FLUORO-1-METHYL-1H-INDOLE-3-CARBALDEHYDE is a derivative of the indole class of compounds, which are known for their diverse range of biological activities. Due to its unique structure and properties, 5-FLUORO-1-METHYL-1H-INDOLE-3-CARBALDEHYDE may have potential as a building block for the synthesis of new drugs and research chemicals.
Uses
Used in Pharmaceutical Industry:
5-FLUORO-1-METHYL-1H-INDOLE-3-CARBALDEHYDE is used as a key intermediate in the synthesis of pharmaceuticals for its potential role in the development of new drugs. Its unique structure allows for the creation of various drug candidates with different therapeutic properties.
Used in Agrochemical Industry:
In the agrochemical industry, 5-FLUORO-1-METHYL-1H-INDOLE-3-CARBALDEHYDE is used as a starting material for the synthesis of agrochemicals. Its potential applications include the development of new pesticides, herbicides, and other crop protection agents.
Used in Dye Industry:
5-FLUORO-1-METHYL-1H-INDOLE-3-CARBALDEHYDE is used as a precursor in the production of dyes due to its fluorescent yellow color. It can be utilized in the creation of various dye formulations for different applications, such as textiles, plastics, and printing inks.
Used in Research and Development:
5-FLUORO-1-METHYL-1H-INDOLE-3-CARBALDEHYDE is used as a research chemical for studying its properties and potential applications in various fields. Its unique structure and fluorescent properties make it a valuable tool for scientific research and the development of new technologies.
Check Digit Verification of cas no
The CAS Registry Mumber 441715-30-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,4,1,7,1 and 5 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 441715-30:
(8*4)+(7*4)+(6*1)+(5*7)+(4*1)+(3*5)+(2*3)+(1*0)=126
126 % 10 = 6
So 441715-30-6 is a valid CAS Registry Number.
InChI:InChI=1/C10H8FNO/c1-12-5-7(6-13)9-4-8(11)2-3-10(9)12/h2-6H,1H3
441715-30-6Relevant articles and documents
Synthesis of 3-Formylindoles via Electrochemical Decarboxylation of Glyoxylic Acid with an Amine as a Dual Function Organocatalyst
Lin, Dian-Zhao,Huang, Jing-Mei
supporting information, p. 5862 - 5866 (2019/08/26)
A new method for 3-formalytion of indoles has been developed through electrochemical decarboxylation of glyoxylic acid with the amine as a dual function organocatalyst. The amine facilitated both the electrochemical decarboxylation and the nucleophilic reaction efficiently, whose loading can be as low as 1 mol %. This protocol has a broad range of functional group tolerance under ambient conditions. The gram-scale experiment has shown great potential in the synthetic application of this strategy.
Visible-Light-Mediated α-Oxygenation of 3-(N,N-Dimethylaminomethyl)-Indoles to Aldehydes
Stanek, Filip,Paw?owski, Robert,Mlynarski, Jacek,Stodulski, Maciej
, p. 6624 - 6628 (2018/10/20)
The visible-light-mediated oxygenation of 3-N,N-(dimethylaminomethyl)-indoles bearing various substituents afforded a series of 3-carbaindole derivatives. Herein we describe the reaction scope, a plausible mechanism and a practical application of this transformation in the formal synthesis of (–)-vincorine is described as well.
Indole-substituted hydrazide derivatives and uses thereof
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Paragraph 0306-0309, (2018/11/03)
The invention discloses indole-substituted hydrazide derivatives and a use thereof, concretely relates to novel indole-substituted hydrazide derivatives and a medicinal composition including the abovecompounds, a use of the derivatives and the medicinal composition in the protection of nerve cells, and also relates to a method for preparing the compounds and the medicinal composition, and a use of the compounds and the medicinal composition in the preparation of drugs for treating diseases associated with glutamate excitotoxicity and oxidative stress damage or free radicals, or neurodegenerative diseases, especially the Alzheimer disease.
