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4,5-DIMETHOXY-1H-INDOLE-2-CARBOXYLIC ACID is a chemical compound with the molecular formula C11H11NO4, belonging to the indole class of compounds. It features two methoxy groups and a carboxylic acid group, which contribute to its unique chemical properties and potential applications. As a versatile building block in organic synthesis, it has garnered interest for its use in the development of pharmaceuticals, agrochemicals, and other advanced materials.

50536-49-7

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50536-49-7 Usage

Uses

Used in Pharmaceutical Industry:
4,5-DIMETHOXY-1H-INDOLE-2-CARBOXYLIC ACID is used as a key intermediate in the synthesis of various pharmaceuticals for its potential biological activities. It has been studied for its potential as an anti-cancer agent, targeting different types of cancer cells, and as a neuroprotective compound, offering therapeutic benefits in neurological disorders.
Used in Agrochemical Industry:
In the agrochemical sector, 4,5-DIMETHOXY-1H-INDOLE-2-CARBOXYLIC ACID is utilized as a precursor in the production of agrochemicals, such as pesticides and herbicides. Its unique chemical structure allows for the development of effective and targeted agrochemicals to protect crops and enhance agricultural productivity.
Used in Material Science:
4,5-DIMETHOXY-1H-INDOLE-2-CARBOXYLIC ACID is employed as a component in the development of new materials, such as organic polymers and composites. Its chemical properties enable the creation of materials with specific characteristics, such as improved stability, enhanced conductivity, or tailored optical properties.
Used in Organic Electronics:
In the field of organic electronics, 4,5-DIMETHOXY-1H-INDOLE-2-CARBOXYLIC ACID is used as a building block for the design and synthesis of organic semiconductors. Its incorporation into organic electronic devices, such as organic light-emitting diodes (OLEDs) and organic solar cells, can potentially improve device performance and efficiency.
Overall, 4,5-DIMETHOXY-1H-INDOLE-2-CARBOXYLIC ACID is a versatile chemical compound with a wide range of applications across various industries, including pharmaceuticals, agrochemicals, material science, and organic electronics. Its unique structure and potential biological activities make it a promising candidate for further research and development.

Check Digit Verification of cas no

The CAS Registry Mumber 50536-49-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,0,5,3 and 6 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 50536-49:
(7*5)+(6*0)+(5*5)+(4*3)+(3*6)+(2*4)+(1*9)=107
107 % 10 = 7
So 50536-49-7 is a valid CAS Registry Number.
InChI:InChI=1/C11H11NO4/c1-15-9-4-3-7-6(10(9)16-2)5-8(12-7)11(13)14/h3-5,12H,1-2H3,(H,13,14)

50536-49-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 4,5-DIMETHOXY-1H-INDOLE-2-CARBOXYLIC ACID

1.2 Other means of identification

Product number -
Other names 4-Methoxy-5-methyl-indol-2-carbonsaeure

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:50536-49-7 SDS

50536-49-7Relevant academic research and scientific papers

Effects of indole fatty alcohols on the differentiation of neural stem cell derived neurospheres

Coowar, Djalil,Bouissac, Julien,Hanbali, Mazen,Paschaki, Marie,Mohier, Eliane,Luu, Bang

, p. 6270 - 6282 (2007/10/03)

In a search for inducers of neuronal differentiation to treat neurodegenerative diseases such as Alzheimer's disease, a series of indole fatty alcohols (IFAs) were prepared, 13c (n = 18) was able to promote the differentiation of neural stem cell derived neurospheres into neurons at a concentration of 10 nM. Analysis of the expression of the Notch pathway genes in neurospheres treated during the differentiation phase with 13c (n = 18) revealed a significant decrease in the transcription of the Notch 4 receptor.

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