112919-69-4 Usage
Uses
Used in Pharmaceutical Research:
1H-Indol-6-ol, 5-methoxy-, acetate (ester) is used as a research compound for its potential pharmacological properties, including anti-inflammatory and antitumor activities. It is being studied for its potential use in the treatment of various medical conditions, such as cancer and neurological disorders.
Used in Organic Synthesis:
1H-Indol-6-ol, 5-methoxy-, acetate (ester) is used as a key intermediate in the synthesis of various organic compounds, contributing to the development of new pharmaceuticals and other chemical products.
With its potential for further research and development, 1H-Indol-6-ol, 5-methoxy-, acetate (ester) holds promise in the pharmaceutical industry for the creation of novel treatments and therapeutic agents.
Check Digit Verification of cas no
The CAS Registry Mumber 112919-69-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,2,9,1 and 9 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 112919-69:
(8*1)+(7*1)+(6*2)+(5*9)+(4*1)+(3*9)+(2*6)+(1*9)=124
124 % 10 = 4
So 112919-69-4 is a valid CAS Registry Number.
112919-69-4Relevant academic research and scientific papers
Product based on inorganic or organic lamellar particles, containing a melanotic pigment, process for preparing it and its use in cosmetics
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, (2008/06/13)
The invention relates to a product in powder form consisting of organic or inorganic particles having a lamellar structure, having a size of less than 50 microns and containing at least one synthetic melanotic pigment formed in situ by oxidation of an indole compound, and to its use for the protection of the human epidermis, in make-up products and for dyeing hair.
Improved Synthesis of 6-Hydroxy-5-methoxy- and 5-Hydroxy-6-methoxyindoles and Their O-Acetates, Analogs of Natural Eumelanin Precursors.
Rogers, C. Bradford,Blum, Charles A.,Murphy, Bryan P.
, p. 941 - 943 (2007/10/02)
Improved routes for syntheses of gram quantities of the isomeric 5,6-acetoxymethoxyindoles, and milligram amounts of the 5,6-hydroxymethoxyindoles, have been developed.They depend on regiospecific nitration of the benzyl ethers of vanillin and isovanillin
