78440-76-3 Usage
Uses
Used in Pharmaceutical Industry:
3-Methoxymethylindole is used as a pharmaceutical compound for its demonstrated antioxidant and anti-inflammatory properties. These characteristics make it a valuable asset in the development of medications targeting a range of conditions that involve oxidative stress and inflammation.
Used in Medicinal Chemistry Research:
In the field of medicinal chemistry, 3-Methoxymethylindole serves as a subject of interest for its potential to contribute to the discovery and design of new drugs. Its unique structure allows researchers to explore its interactions with biological targets and its potential to be modified for enhanced therapeutic effects.
Used as a Precursor in Organic Synthesis:
3-Methoxymethylindole is utilized as a precursor in the synthesis of other chemical compounds. Its presence in the molecular structure of various target compounds makes it a key component in organic synthesis processes, facilitating the creation of new molecules with specific applications in different industries.
Check Digit Verification of cas no
The CAS Registry Mumber 78440-76-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,4,4 and 0 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 78440-76:
(7*7)+(6*8)+(5*4)+(4*4)+(3*0)+(2*7)+(1*6)=153
153 % 10 = 3
So 78440-76-3 is a valid CAS Registry Number.
InChI:InChI=1/C10H11NO/c1-12-7-8-6-11-10-5-3-2-4-9(8)10/h2-6,11H,7H2,1H3
78440-76-3Relevant academic research and scientific papers
A SYNTHESIS METHOD OF INDOLE-3-METHANAMINE AND/OR GRAMINE FROM INDOLE-3-CARBOXALDEHYDE, AND ITS APPLICATION FOR THE SYNTHESES OF BRASSININ, ITS 4-SUBSTITUTED ANALOGS, AND 1,3,4,5-TETRAHYDROPYRROLOQUINOLINE
Yamada, Fumio,Kobayashi, Kensuke,Shimizu, Aya,Aoki, Naokatsu,Somei, Masanori
, p. 2783 - 2804 (2007/10/02)
Simple conversion method of indole-3-carboxaldehyde into gramine and/or indole-3-methanamine was developed.The present method realized short step syntheses of brassinin, 4-iodo-, methoxy-, 4-methoxy, and 4-nitrobrassinin, 4-methoxyindole-3-acetonitrile, and 1,3,4,5-tetrahydropyrroloquinoline.
