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2-(dimethylamino)-1-(1-ethyl-1H-indol-3-yl)ethanol is a versatile chemical compound belonging to the class of amino alcohols. It features a dimethylamino group attached to the second carbon of a 1-(1-ethyl-1H-indol-3-yl)ethanol molecule, which endows it with unique structural and functional properties. 2-(dimethylamino)-1-(1-ethyl-1H-indol-3-yl)ethanol is widely recognized for its potential as a chiral auxiliary and its ability to serve as a ligand in metal-catalyzed reactions. Additionally, it exhibits pharmacological properties, positioning it as a valuable molecule for the development of new drugs across various scientific fields.

5135-83-1

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5135-83-1 Usage

Uses

Used in Organic Synthesis:
2-(dimethylamino)-1-(1-ethyl-1H-indol-3-yl)ethanol is used as a chiral auxiliary in organic synthesis for its ability to influence the stereochemistry of chemical reactions, leading to the production of enantiomerically pure compounds. This is crucial in the synthesis of pharmaceuticals and other chiral molecules where stereochemistry plays a significant role in biological activity.
Used in Pharmaceutical Research:
In pharmaceutical research, 2-(dimethylamino)-1-(1-ethyl-1H-indol-3-yl)ethanol is utilized as a ligand in metal-catalyzed reactions, facilitating the development of novel synthetic routes and methodologies. Its role in these reactions can enhance the efficiency and selectivity of the synthesis of bioactive compounds, contributing to the discovery of new drugs.
Used in Drug Development:
2-(dimethylamino)-1-(1-ethyl-1H-indol-3-yl)ethanol is employed in drug development due to its inherent pharmacological properties. Its unique structure allows it to interact with biological targets, potentially leading to the creation of new therapeutic agents with improved efficacy and selectivity.
Used in Chemical Research:
In the broader field of chemical research, 2-(dimethylamino)-1-(1-ethyl-1H-indol-3-yl)ethanol serves as a model compound for studying the effects of structural modifications on the properties and reactivity of amino alcohols. This contributes to the fundamental understanding of molecular interactions and the design of new chemical entities with tailored properties for specific applications.
Used in Analytical Chemistry:
2-(dimethylamino)-1-(1-ethyl-1H-indol-3-yl)ethanol can be used in analytical chemistry as a chiral selector in techniques such as chromatography and capillary electrophoresis. Its ability to differentiate between enantiomers is valuable for the separation and analysis of chiral compounds in various industries, including pharmaceuticals and agrochemicals.

Check Digit Verification of cas no

The CAS Registry Mumber 5135-83-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,1,3 and 5 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 5135-83:
(6*5)+(5*1)+(4*3)+(3*5)+(2*8)+(1*3)=81
81 % 10 = 1
So 5135-83-1 is a valid CAS Registry Number.

5135-83-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(dimethylamino)-1-(1-ethylindol-3-yl)ethanol

1.2 Other means of identification

Product number -
Other names 1-(1-Aethyl-indol-3-yl)-2-dimethylamino-aethanol

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:5135-83-1 SDS

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