118573-52-7 Usage
Uses
Used in Pharmaceutical Industry:
1H-Indole-3-acetonitrile, 4-hydroxyis used as an anti-cancer agent for its ability to inhibit the growth of certain cancer cells. It has shown potential in targeting and disrupting the mechanisms of cancer cell proliferation and survival, offering a promising avenue for cancer treatment.
Used in Antibacterial Applications:
1H-Indole-3-acetonitrile, 4-hydroxyis used as an antibacterial agent due to its ability to combat bacterial infections. Its mechanism of action may involve disrupting bacterial cell walls or inhibiting essential bacterial enzymes, thereby reducing the viability of pathogenic bacteria.
Used in Antifungal Applications:
1H-Indole-3-acetonitrile, 4-hydroxyis utilized as an antifungal agent, effective against various fungal species. It may act by interfering with fungal cell membrane integrity or by inhibiting key enzymes necessary for fungal growth and reproduction.
Used in Synthesis of Pharmaceutical Compounds:
As a precursor in the synthesis of various pharmaceutical compounds, 1H-Indole-3-acetonitrile, 4-hydroxyplays a crucial role in the development of new drugs. Its unique chemical structure allows for the creation of diverse molecules with potential therapeutic applications, contributing to the advancement of medicinal chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 118573-52-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,8,5,7 and 3 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 118573-52:
(8*1)+(7*1)+(6*8)+(5*5)+(4*7)+(3*3)+(2*5)+(1*2)=137
137 % 10 = 7
So 118573-52-7 is a valid CAS Registry Number.
118573-52-7Relevant academic research and scientific papers
The first and simple total synthesis of cappariloside A1
Somei, Masanori,Yamada, Fumio
, p. 1573 - 1578 (2007/10/03)
A lithium hydroxide promoted simple glycosylation of 4-hydroxyindole-3- acetonitrile with 2,3,4, 6-tetra-O-acetyl-a-D-glucopyranosyl bromide was developed. Utilizing the method, the first and five steps total synthesis of cappariloside A was achieved from indole-3-carbaldehyde in 41% overall yield.
