151320-84-2 Usage
Molecular Structure
1H-Indole-7-carboxaldehyde, 4,6-dimethoxy-3-(4-methoxyphenyl)consists of an indole ring, a carboxaldehyde group, and dimethoxy and methoxyphenyl substituents.
Indole Ring
The indole ring is a core structure in many biologically active compounds and is known for its aromatic properties.
Carboxaldehyde Group
The presence of a carboxaldehyde group (-CHO) imparts aldehyde-like reactivity, making it susceptible to nucleophilic addition and oxidation reactions.
Dimethoxy Substituents
Two methoxy groups (-OCH3) are attached to the indole ring, which can influence the electronic and steric properties of the molecule.
Methoxyphenyl Substituent
A 4-methoxyphenyl group is attached to the indole ring, further contributing to the molecule's electronic and steric properties.
Potential Applications
Due to its diverse structural features, 1H-Indole-7-carboxaldehyde, 4,6-dimethoxy-3-(4-methoxyphenyl)may have potential applications in pharmaceuticals, agrochemicals, and materials science.
Synthesis Building Block
The specific properties and reactivity of 1H-Indole-7-carboxaldehyde, 4,6-dimethoxy-3-(4-methoxyphenyl)- make it a valuable building block for the synthesis of more complex organic molecules and materials.
Further Research
Additional research and exploration of 1H-Indole-7-carboxaldehyde, 4,6-dimethoxy-3-(4-methoxyphenyl)-'s potential applications are needed to fully understand and harness its properties.
Check Digit Verification of cas no
The CAS Registry Mumber 151320-84-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,1,3,2 and 0 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 151320-84:
(8*1)+(7*5)+(6*1)+(5*3)+(4*2)+(3*0)+(2*8)+(1*4)=92
92 % 10 = 2
So 151320-84-2 is a valid CAS Registry Number.
151320-84-2Relevant academic research and scientific papers
The nitration of some 4,6-dimethoxyindoles
Jones, Ashley W.,Purwono, Bambang,Bowyer, Paul K.,Mitchell, Peter S.R.,Kumar, Naresh,Nugent, Stephen J.,Jolliffe, Katrina A.,Black, David StC.
, p. 10779 - 10786 (2007/10/03)
A range of 3-substituted-4,6-dimethoxyindoles bearing electron-withdrawing groups in either the 2- or 7-position, can be nitrated using nitric acid adsorbed on silica, to give 7-nitro and 2-nitro-indoles, respectively. A 1-cyano-indole gives regioselectiv
Calixindoles, New Macrocyclic Tris(indolylmethylene) Compounds with 2,7-Linkages
Black, David St. C.,Bowyer, Michael C.,Kumar, Naresh,Mitchell, Peter S. R.
, p. 819 - 821 (2007/10/02)
A series of macrocyclic tris(indolylmethylene) compounds (calixindoles> can be obtained from 7- or 2-hydroxymethylindoles or from the combination of either an indole with a bis(hydroxymethyl)-2,7'-diindolylmethane or a bis(hydroxymethyl)indole with a 2,7'-diindolylmethane; an isomeric series can be obtained from the combination of an indole with a bis(hydroxymethyl)-2,2'-diindolylmethane.
