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5-ETHOXY-1H-INDOLE-3-CARBALDEHYDE is a chemical compound that belongs to the class of indole carbaldehydes. It is a derivative of indole, which is a heterocyclic aromatic organic compound. 5-ETHOXY-1H-INDOLE-3-CARBALDEHYDE is characterized by the presence of an ethoxy group and a carbonyl group attached to the indole ring. It is commonly used as an intermediate in the synthesis of various pharmaceuticals and biologically active molecules. Additionally, it exhibits interesting pharmacological properties and is being studied for its potential applications in the field of medicinal chemistry.

169789-47-3

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169789-47-3 Usage

Uses

Used in Pharmaceutical Industry:
5-ETHOXY-1H-INDOLE-3-CARBALDEHYDE is used as an intermediate in the synthesis of various pharmaceuticals and biologically active molecules. Its unique chemical structure allows it to be a key component in the development of new drugs and therapeutic agents.
Used in Medicinal Chemistry Research:
5-ETHOXY-1H-INDOLE-3-CARBALDEHYDE is used as a subject of study in medicinal chemistry research. Its interesting pharmacological properties make it a promising candidate for the development of new drugs and therapeutic agents. Researchers are exploring its potential applications in various areas of medicine, including the treatment of diseases and disorders.
Used in Chemical Synthesis:
5-ETHOXY-1H-INDOLE-3-CARBALDEHYDE is used as a building block in the chemical synthesis of various compounds. Its versatile chemical structure allows it to be modified and combined with other molecules to create new compounds with specific properties and functions.
Used in Drug Development:
5-ETHOXY-1H-INDOLE-3-CARBALDEHYDE is used in drug development as a potential lead compound. Its unique chemical properties and pharmacological activities make it a valuable starting point for the design and development of new drugs and therapeutic agents.
Used in Biochemical Research:
5-ETHOXY-1H-INDOLE-3-CARBALDEHYDE is used in biochemical research to study its interactions with biological systems and to understand its potential effects on various biological processes. This research can provide valuable insights into the compound's mechanism of action and its potential applications in medicine and other fields.

Check Digit Verification of cas no

The CAS Registry Mumber 169789-47-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,9,7,8 and 9 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 169789-47:
(8*1)+(7*6)+(6*9)+(5*7)+(4*8)+(3*9)+(2*4)+(1*7)=213
213 % 10 = 3
So 169789-47-3 is a valid CAS Registry Number.
InChI:InChI=1/C11H11NO2/c1-2-14-9-3-4-11-10(5-9)8(7-13)6-12-11/h3-7,12H,2H2,1H3

169789-47-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-ETHOXY-1H-INDOLE-3-CARBALDEHYDE

1.2 Other means of identification

Product number -
Other names 5-Ethoxyindole-3-carboxaldehyde

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:169789-47-3 SDS

169789-47-3Downstream Products

169789-47-3Relevant academic research and scientific papers

The serotonin 5-HT4 receptor. 2. Structure-activity studies of the indole carbazimidamide class of agonists.

Buchheit,Gamse,Giger,Hoyer,Klein,Kloeppner,Pfannkuche,Mattes

, p. 2331 - 2338 (2007/10/02)

A number of substituted indole carbazimidamides were prepared and evaluated as 5-HT4 receptor agonists by using the isolated field-stimulated guinea pig ileum preparation. Their selectivity for the 5-HT4 receptor was established by examining their affinity for other 5-HT receptors using radioligand-binding techniques. Several selective and highly potent full as well as partial agonists emerged from this study. For example, 1b,d were found to be the most potent, full 5-HT4 receptor agonist described so far (EC50 = 0.5 and 0.8 nM, respectively), being 6 and 4 times more potent than serotonin itself. On the other hand, 5b and 1h appeared as partial 5-HT4 receptor agonists in the nonstimulated guinea pig ileum preparation with potencies, evaluated against serotonin action, respectively similar (5b, Ki = 12 nM) to and 300-fold higher (1h, Ki = 0.04 nM) than serotonin.

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