147591-43-3 Usage
Derivative of
Indole
Benzyl group
Attached to the 1-position
Methyl group
At the 2-position
Nitro group
At the 3-position
Hydroxy group
At the 5-position
Usage
Organic synthesis and pharmaceutical research
Reactivity
Versatile
Potential
Biological activity
Applications
Development of new drugs and as a building block for complex molecules
Chemical properties
Influenced by nitro and hydroxy groups
Biological properties
Unique due to nitro and hydroxy groups
Role
Valuable tool in medicinal chemistry and chemical biology
Significance
Potential in development of new therapeutic agents and biologically active compounds
Check Digit Verification of cas no
The CAS Registry Mumber 147591-43-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,7,5,9 and 1 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 147591-43:
(8*1)+(7*4)+(6*7)+(5*5)+(4*9)+(3*1)+(2*4)+(1*3)=153
153 % 10 = 3
So 147591-43-3 is a valid CAS Registry Number.
147591-43-3Relevant academic research and scientific papers
Quinoneimines in the Nenitzescu reaction
Lyubchanskaya,Panisheva,Savina,Alekseeva,Shashkov,Granik
, p. 1690 - 1699 (2007/10/03)
The Nenitzescu reaction involving quinoneimines was studied; new 5-aminoindole, 5-aminobenzofuran, and 9-aminochromenopyridine derivatives were synthesized.
LACTAM AND ACID AMIDE ACETALS. 71. NEW SYNTHESIS OF 3-NITRO-6-HYDROXYINDOLE DERIVATIVES
Lyubchanskaya, V. M.,Alekseeva, L. M.,Granik, V. G.
, p. 34 - 39 (2007/10/02)
Previously unknown 3-nitro-6-hydroxyindole derivatives were synthesized by condensation of p-benzoquinone with secondary β-nitro enamines.
