123797-41-1 Usage
Derivative of indole
It is based on the indole structure, which is a heterocyclic aromatic organic compound.
Contains two phenylmethylene groups
The compound has two phenylmethylene (C6H5-CH2-) groups attached to its structure.
Methylated indole ring
The indole ring in the compound has a methyl (-CH3) group attached to it.
Complex molecule
The compound has a complex structure due to the presence of multiple functional groups.
Potential applications in organic chemistry and pharmacology
The compound's unique structure and properties make it an interesting target for further study and potential development in these fields.
Interesting target for new chemical and pharmaceutical applications
The compound's structure and properties may lead to the development of new applications in the chemical and pharmaceutical industries.
Check Digit Verification of cas no
The CAS Registry Mumber 123797-41-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,3,7,9 and 7 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 123797-41:
(8*1)+(7*2)+(6*3)+(5*7)+(4*9)+(3*7)+(2*4)+(1*1)=141
141 % 10 = 1
So 123797-41-1 is a valid CAS Registry Number.
123797-41-1Relevant academic research and scientific papers
Black, David St. C.,Craig, Donald C.,Kumar, Naresh
, p. 425 - 426 (1989)
4,6-Dimethoxy-3-methylindole can be converted by treatment with aryl aldehydes and phosphoryl chloride in chloroform into macrocyclic tri-indolyl methanes, with the indole rings linked at C-2 and C-7.
Reaction of 4,6-dimethoxy-3-methylindole with aromatic aldehydes: A simple synthesis of calix[3]indoles
Black, David St.C.,Craig, Donald C.,Kumar, Naresh
, p. 311 - 318 (2007/10/03)
2,7:2,7:2,7-Linked calix[3]indoles (3a-d) have been prepared by the reaction of 4,6-dimethoxy-3-methylindole (1) and benzaldehydes with phosphoryl chloride or by a direct reaction of di(4,6-dimethoxy-3-methylindol-2-yl)phenylmethanes (2a-d) with phosphoryl chloride. An X-ray crystal structure determination of the macrocycle (3d) is reported. 4,6-Dimethoxy-3-methylindolemethanols (9) and (10) were prepared and reacted with phosphoryl chloride to study the mechanism of formation of the macrocycle.
