175913-29-8 Usage
Description
5-Methoxy-6-nitro-1H-indole is a nitroindole derivative characterized by a molecular formula of C9H7NO3. It features an indole ring structure with a methoxy group at the 5th position and a nitro group at the 6th position. This chemical compound serves as a versatile building block in the synthesis of pharmaceuticals and organic compounds, and it has been explored for its potential biological and pharmacological properties, such as anti-inflammatory and antitumor activities.
Uses
Used in Pharmaceutical Synthesis:
5-Methoxy-6-nitro-1H-indole is used as a key intermediate in the synthesis of various pharmaceuticals and organic compounds. Its unique structure allows for the creation of a wide range of molecules with diverse therapeutic applications.
Used in Medicinal Chemistry Research:
In the field of medicinal chemistry, 5-Methoxy-6-nitro-1H-indole is utilized as a starting material for the development of new drugs. Its chemical properties make it a promising candidate for the design of molecules with improved pharmacological profiles.
Used in Anti-inflammatory Applications:
5-Methoxy-6-nitro-1H-indole has been investigated for its anti-inflammatory properties. It may be used as a therapeutic agent to alleviate inflammation and associated symptoms in various conditions.
Used in Antitumor Applications:
5-Methoxy-6-nitro-1H-indole has also shown potential in antitumor research. 5-Methoxy-6-nitro-1H-indole may be employed as an anticancer agent, targeting tumor cells and inhibiting their growth and proliferation.
Used in Drug Development:
In the pharmaceutical industry, 5-Methoxy-6-nitro-1H-indole is used as a lead compound in drug development. Its unique chemical structure and biological activities make it a valuable asset in the discovery and optimization of new therapeutic agents.
Used in Organic Chemistry Research:
5-Methoxy-6-nitro-1H-indole is also utilized in organic chemistry research to study the reactivity and functionalization of indole rings. This knowledge can be applied to the development of new synthetic methods and the synthesis of novel organic compounds.
Check Digit Verification of cas no
The CAS Registry Mumber 175913-29-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,5,9,1 and 3 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 175913-29:
(8*1)+(7*7)+(6*5)+(5*9)+(4*1)+(3*3)+(2*2)+(1*9)=158
158 % 10 = 8
So 175913-29-8 is a valid CAS Registry Number.
175913-29-8Relevant articles and documents
Efficient mononitration of indolic compounds with nitric acid impregnated on silica gel
Roué, Nathalie,Delahaigue, Thierry,Barret, Roland
, p. 263 - 266 (1996)
The methoxyindoles (N-benzenesulfonyl and 2-carbomethoxy) were mononitrated with nitric acid adsorbed on silica gel under mild conditions to give mononitroindoles in good chemical yields.
