201486-54-6 Usage
Derived from indole
1H-Indole, 1-(2,4-dimethoxybenzoyl)is a chemical compound that is derived from indole, a bicyclic organic compound that is widely found in nature.
Bicyclic structure
The compound has a bicyclic structure, which is a common feature of indole-based compounds.
2,4-dimethoxybenzoyl moiety
The addition of a 2,4-dimethoxybenzoyl group to the indole core results in a compound with potential pharmaceutical and industrial applications.
Potential pharmaceutical applications
1H-Indole, 1-(2,4-dimethoxybenzoyl)has been studied for its potential use in the development of new drugs due to its diverse biological activities, including antitumor, anti-inflammatory, and antimicrobial properties.
Industrial applications
The presence of the 2,4-dimethoxybenzoyl group may make this compound useful for industrial applications such as in the production of dyes, fragrances, and other chemical products.
Further research needed
Further research and development of this compound could uncover more of its potential uses and benefits.
Check Digit Verification of cas no
The CAS Registry Mumber 201486-54-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,1,4,8 and 6 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 201486-54:
(8*2)+(7*0)+(6*1)+(5*4)+(4*8)+(3*6)+(2*5)+(1*4)=106
106 % 10 = 6
So 201486-54-6 is a valid CAS Registry Number.
201486-54-6Relevant articles and documents
2-(2-aminophenyl)-acetaldehyde dimethyl acetal: A novel reagent for the protection of carboxylic acids
Arai, Eri,Tokuyama, Hidetoshi,Linsell, Martin S.,Fukuyama, Tohru
, p. 71 - 74 (2007/10/03)
The synthesis and use of 2-(2-aminophenyl)-acetaldehyde dimethyl acetal 1 are described. The amides 2, derived from this amine and carboxylic acids, are stable under basic conditions and thus can be regarded as the protected carboxylic acids. The corresponding carboxylic acids are regenerated by conversion of 2 into indolylamides 3 by treatment with CSA and subsequent hydrolysis with LiOOH or NaOH. In addition, 3 can be easily converted to esters, amides, and aldehydes.
