6116-77-4 Usage
Heterocyclic organic compound
The chemical 4H-Indol-4-one, 2-ethyl-1,5,6,7-tetrahydro-3-methylis a compound that contains a ring structure containing both carbon and non-carbon atoms.
Derivative of indole
4H-Indol-4-one,2-ethyl-1,5,6,7-tetrahydro-3-methyl- is derived from the indole structure, which is commonly found in many natural products.
Ethyl and methyl group substitution
The compound has an ethyl group (C2H5) and a methyl group (CH3) attached to the indolone ring, which can affect its chemical properties and reactivity.
Tetrahydro substitution
The compound has a tetrahydro substitution at position 1,5,6, and 7, which means that four hydrogen atoms have replaced four carbon atoms in the indolone ring, changing its chemical properties.
Building block in synthesis
4H-Indol-4-one,2-ethyl-1,5,6,7-tetrahydro-3-methyl- is often used as a building block in the synthesis of various pharmaceuticals and biologically active compounds due to its unique structure and reactivity.
Potential applications in agrochemicals and materials science
Due to its diverse chemical properties, 4H-Indol-4-one,2-ethyl-1,5,6,7-tetrahydro-3-methyl- may have potential applications in the development of agrochemicals and materials for various uses.
Check Digit Verification of cas no
The CAS Registry Mumber 6116-77-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,1,1 and 6 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 6116-77:
(6*6)+(5*1)+(4*1)+(3*6)+(2*7)+(1*7)=84
84 % 10 = 4
So 6116-77-4 is a valid CAS Registry Number.
6116-77-4Relevant academic research and scientific papers
Urea decomposition: Efficient synthesis of pyrroles using the deep eutectic solvent choline chloride/urea
Hu, Lanfang,Luo, Juan,Lu, Dan,Tang, Qiang
, p. 1698 - 1701 (2018/04/02)
A simple and efficient method is reported for the synthesis of pyrroles via condensation of a series of tricarbonyl compounds with ammonia, which was generated in situ from decomposition of the deep eutectic solvent choline chloride/urea.
