61995-50-4 Usage
Molecular structure
1H-Indole, 3,3'-methylenebis[2-methylconsists of an indole molecule with two methyl groups attached through a methylene bridge.
Aromatic compound
Indole is a heterocyclic aromatic compound that is commonly found in various plants.
Industrial applications
Indole has applications in the pharmaceutical and chemical industries.
Stability
The addition of two methyl groups to the indole molecule increases its stability.
Organic synthesis
The compound is more suitable for use in organic synthesis due to its increased stability.
Building block
The compound can serve as a building block for more complex compounds.
Potential applications
The 3,3'-methylenebis[2-methylderivative of indole may have potential applications in medicine, agriculture, or other fields due to its unique chemical structure and properties.
Chemical and physical properties
Understanding the properties of 1H-Indole, 3,3'-methylenebis[2-methylcan provide insights into its potential uses and applications in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 61995-50-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,9,9 and 5 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 61995-50:
(7*6)+(6*1)+(5*9)+(4*9)+(3*5)+(2*5)+(1*0)=154
154 % 10 = 4
So 61995-50-4 is a valid CAS Registry Number.
61995-50-4Relevant academic research and scientific papers
Nitrenium Ions. Part 1. Acid-catalysed Reactions of 2-Methylindole with Nitrosobenzenes. Crystal Structures of 2-Phenylamino-3-phenylimino-3H-indole, 2-(o-Tolylamino)-3-(o-tolylimino)-3H-indole, N-Phenyl-N-(2-phenylamino-3H-indol-3-ylidene)amine N-Oxide and Bis(2-methyl-1H-indol-3-yl)...
Cardellini, Liberato,Carloni, Patricia,Damiani, Elisabetta,Greci, Lucedio,Stipa, Pierluigi,et al.
, p. 1589 - 1596 (2007/10/02)
2-Methylindole 3b reacts with nitrosobenzenes 1a-c in the presence of monochloroacetic acid affording compounds which are characterized by the formation of carbon-nitrogen bonds and other compounds which clearly could arise from a radical mechanism.The radical component of the reaction is also supported by the EPR spectroscopy as well as the reaction products distribution.Although these reactions cannot be considered of synthetic value for the number of isolated products, they could be regarded as clear examples of the electrophilic character and of the oxidative power of nitrogen in activated nitrosobenzenes.Crystal structures of 2-phenylamino-3-phenylimino-3H-indole 7a, 2-(o-tolylamino)-3-(o-tolylimino)-3H-indole 7b, N-phenyl-N-(2-phenylamino-3H-indol-3-ylidene)amine N-oxide 9a and bis(2-methyl-1H-indol-3-yl)methane 10 are also reported.
