126309-77-1 Usage
Derivative of indole
A heterocyclic aromatic compound
Contains a 3-chloro-1-methyl group
A chlorine atom attached to the third carbon and a methyl group attached to the first carbon
Commonly used in synthesis
Used in the production of pharmaceuticals, agrochemicals, and other organic compounds
Potential antibacterial and antifungal properties
Has been studied for its ability to inhibit the growth of bacteria and fungi
Derivatives have shown potential for treating various diseases and medical conditions
Variants of 1H-Indole-2-carboxaldehyde, 3-chloro-1-methyl- have demonstrated potential for therapeutic use
Used in development of fluorescent probes and dyes for biological imaging and diagnostics
Utilized in creating compounds that can be used to visualize and diagnose biological processes and conditions.
Check Digit Verification of cas no
The CAS Registry Mumber 126309-77-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,6,3,0 and 9 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 126309-77:
(8*1)+(7*2)+(6*6)+(5*3)+(4*0)+(3*9)+(2*7)+(1*7)=121
121 % 10 = 1
So 126309-77-1 is a valid CAS Registry Number.
126309-77-1Relevant academic research and scientific papers
Chemistry of polyhalogenated nitrobutadienes, part 11: Ipso-formylation of 2-chlorothiophenes under Vilsmeier-Haack conditions
Vogt, Eva-Janina,Zapol'skii, Viktor A.,Nutz, Eva,Kaufmann, Dieter E.
experimental part, p. 285 - 294 (2012/07/14)
The regioselective ipso-formylation of electron-rich, 3,4-push-pull- substituted 2-chlorothiophenes under Vilsmeier-Haack conditions was performed in good yields. The synthetic scope of this new reaction was explored using various halothiophenes, chloroanilines, and 1-methyl-3-chloroindole. In comparison with their structural C-H analogs the chlorinated thiophenes, anilines, and the indole proved to be less reactive toward electrophilic attack by chloromethyleniminium salts.