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2-(diethylamino)-1-(1H-indol-3-yl)ethanone is a synthetic chemical compound characterized by the molecular formula C16H21NO. It features an indole ring and an ethanone functional group, which contribute to its potential pharmacological properties. 2-(diethylamino)-1-(1H-indol-3-yl)ethanone is of interest in research and pharmaceutical applications due to its possible interactions with neurotransmitter receptors in the brain, suggesting its potential to influence mood, cognition, and behavior.

92292-25-6

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92292-25-6 Usage

Uses

Used in Pharmaceutical Research and Development:
2-(diethylamino)-1-(1H-indol-3-yl)ethanone is utilized as a key intermediate in the synthesis of new drugs and treatments. Its unique structure and properties make it a promising candidate for the development of medications targeting various neurological and psychiatric conditions.
Used in Neurotransmitter Receptor Research:
In the field of neuroscience, 2-(diethylamino)-1-(1H-indol-3-yl)ethanone is employed as a research tool to study the interactions between neurotransmitter receptors and potential modulating agents. This helps in understanding the mechanisms of action and the therapeutic potential of 2-(diethylamino)-1-(1H-indol-3-yl)ethanone in treating mood disorders, cognitive impairments, and behavioral issues.
Used in Drug Discovery for Neurological Conditions:
2-(diethylamino)-1-(1H-indol-3-yl)ethanone is used as a lead compound in drug discovery programs focused on neurological conditions. Its ability to modulate neurotransmitter receptors suggests that it may play a role in the development of treatments for conditions such as depression, anxiety, schizophrenia, and other mood and cognitive disorders.
Used in Chemical Synthesis for Diverse Applications:
Beyond its pharmaceutical applications, 2-(diethylamino)-1-(1H-indol-3-yl)ethanone can also be used as a building block in the synthesis of various chemical compounds for different industries, including materials science, agrochemicals, and specialty chemicals, where its unique structural features may offer novel properties and functionalities.

Check Digit Verification of cas no

The CAS Registry Mumber 92292-25-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,2,2,9 and 2 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 92292-25:
(7*9)+(6*2)+(5*2)+(4*9)+(3*2)+(2*2)+(1*5)=136
136 % 10 = 6
So 92292-25-6 is a valid CAS Registry Number.

92292-25-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(diethylamino)-1-(1H-indol-3-yl)ethanone

1.2 Other means of identification

Product number -
Other names -

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

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More Details:92292-25-6 SDS

92292-25-6Downstream Products

92292-25-6Relevant academic research and scientific papers

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