770729-12-9 Usage
Derivative of
indol-4-ol
Contains
a methyl group and a phenylmethyl group attached to the indole ring
Potential pharmacological properties
antioxidant, anti-inflammatory, and neuroprotective activities
Possible applications
drug development and medicinal chemistry
Potential use in treatment
cancer, neurodegenerative diseases, and inflammation-related conditions.
Check Digit Verification of cas no
The CAS Registry Mumber 770729-12-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,7,0,7,2 and 9 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 770729-12:
(8*7)+(7*7)+(6*0)+(5*7)+(4*2)+(3*9)+(2*1)+(1*2)=179
179 % 10 = 9
So 770729-12-9 is a valid CAS Registry Number.
770729-12-9Relevant academic research and scientific papers
Synthesis of 5-methylindole-4,7-quinone through a new construction of the functionalized indole ring based on the allene-mediated electrocyclic reaction involving the pyrrole [b]-bond
Hirayama, Maho,Choshi, Tominari,Kumemura, Teppei,Tohyama, Shigeo,Nobuhiro, Junko,Hibino, Satoshi
, p. 1765 - 1770 (2007/10/03)
A new synthesis of an indole ring based on an electrocyclic reaction of a 2-alkenyl-3-allenylpyrrole intermediate generating from 2-ethenyl-3- propargylpyrrole was established. A synthesis of 5-methylindole-4,7-quinone (1) was completed in seven steps from the 4-oxygenated 5-methylindole (13a). It was demonstrated that the structure of natural product (1), isolated from Dropella fragum, is not at least 5-methylindole-4,7-quinone (1).
