4993-92-4 Usage
Uses
Used in Pharmaceutical Synthesis:
1-(6-nitro-1H-indol-3-yl)ethanone is used as an intermediate in the pharmaceutical industry for the synthesis of various pharmaceuticals and organic compounds. Its unique structure, including the nitro group and ketone functional group, allows for the creation of a wide range of molecules with potential therapeutic applications.
Used in Organic Chemistry:
In the field of organic chemistry, 1-(6-nitro-1H-indol-3-yl)ethanone serves as a valuable building block for the synthesis of diverse organic compounds. Its functional groups can be manipulated to produce a variety of molecules with different properties and potential uses.
Used in Biological and Pharmacological Research:
1-(6-nitro-1H-indol-3-yl)ethanone is also utilized in biological and pharmacological research to explore its potential effects on various biological systems. Although its specific activities have not been fully determined, ongoing studies may reveal new applications and uses for 1-(6-nitro-1H-indol-3-yl)ethanone in the future.
Check Digit Verification of cas no
The CAS Registry Mumber 4993-92-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,9,9 and 3 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 4993-92:
(6*4)+(5*9)+(4*9)+(3*3)+(2*9)+(1*2)=134
134 % 10 = 4
So 4993-92-4 is a valid CAS Registry Number.
InChI:InChI=1/C10H8N2O3/c1-6(13)9-5-11-10-4-7(12(14)15)2-3-8(9)10/h2-5,11H,1H3
4993-92-4Relevant academic research and scientific papers
Regioselective nitration of 3-acetylindole and its N-acyl and N-sulfonyl derivatives
Ottoni, Olivia,Cruz, Rosimeire,Krammer, Norbert H.
, p. 1117 - 1120 (2007/10/03)
3-Acetylindole reacts regioselectively with NO2BF4 in the presence of SnCl4 to produce 3-acetyl-5-nitroindole or 3-acetyl-6-nitroindole, depending on the temperature, both in excellent yields.
INTERACTION OF INDOLES WITH GLYCOSYL HALIDES IN THE PRESENCE OF SILVER OXIDE
Sokolova, Tatiana N.,Shevchenko, Valery E.,Preobrazhenskaya, Maria N.
, p. 249 - 262 (2007/10/02)
The reaction of indole with 2,3,4-tri-O-acetyl-β-L-arabinopyranosyl bromide in the presence of silver oxide yielded a mixture of O-acetylated 1-α-L-arabinopyranosylindole, 3-α-L-arabinopyranosylindole (the first indole C-nucleoside), and 1,2-O-1-(indol-1
