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2-(5-Chloro-1H-indol-3-yl)ethanamine hydrochloride

Basic Information

  • CAS No.: 942-26-7
  • Purity: 99%
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Details

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1.What is the 2-(5-Chloro-1H-indol-3-yl)ethanamine hydrochloride ?

Used in Pharmaceutical Research:
2-(5-Chloro-1H-indol-3-yl)ethanamine hydrochloride is utilized as a research chemical for exploring its potential applications in the pharmaceutical industry. Its diverse properties and interactions with biological targets make it a candidate for further investigation into its therapeutic effects and mechanisms of action.
Used in Laboratory Settings:
In the laboratory, 2-(5-Chloro-1H-indol-3-yl)ethanamine hydrochloride is used as a stable compound for conducting experiments and studies. Its hydrochloride salt form ensures that it remains stable under controlled conditions, facilitating its use in a variety of research applications.
Used in Drug Development:
2-(5-Chloro-1H-indol-3-yl)ethanamine hydrochloride may be employed as a starting material or intermediate in the synthesis of new drugs. Its unique structure and potential to interact with various biological targets could contribute to the development of novel therapeutic agents.
Used in Receptor and Enzyme Interaction Studies:
2-(5-Chloro-1H-indol-3-yl)ethanamine hydrochloride is used in studies aimed at understanding its interactions with different receptors and enzymes in the body. Such research can provide insights into its potential biological activities and help in identifying its role in various physiological or pathological processes.
Further research and investigation are essential to fully comprehend the potential uses and effects of 2-(5-Chloro-1H-indol-3-yl)ethanamine hydrochloride, ensuring its safe and effective application in the relevant fields.

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Conditions
Conditions Yield
With disodium hydrogenphosphate; In ethanol; water; at 75 ℃; for 6h; pH=6 - 7;
12.7 g
3-(2-aminoethyl)-5-chloro-1H-indole-2-carboxylic acid
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Conditions
Conditions Yield
With hydrogenchloride; for 2h; Heating;
72%

2.What is the CAS number for 2-(5-Chloro-1H-indol-3-yl)ethanamine hydrochloride ?

The CAS number of 2-(5-Chloro-1H-indol-3-yl)ethanamine hydrochloride is 942-26-7.

More information of 2-(5-Chloro-1H-indol-3-yl)ethanamine hydrochloride 942-26-7 are:

CAS?Number

942-26-7

Melting Point

290°C (dec.)

Boiling Point

375.7 °C at 760 mmHg

Flash Point

181 °C

Vapor Pressure

7.61E-06mmHg at 25°C

HS CODE

2933990090

PSA

41.81000

LogP

3.82480

3.What are another words for 2-(5-Chloro-1H-indol-3-yl)ethanamine hydrochloride ?

Synonyms?for?2-(5-Chloro-1H-indol-3-yl)ethanamine hydrochloride 942-26-7:1H-Indole-3-ethanamine,5-chloro-, monohydrochloride (9CI);Indole, 3-(2-aminoethyl)-5-chloro-, hydrochloride(6CI,7CI,8CI);5-Chlorotryptamine hydrochloride;1H-Indole-3-ethanamine, 5-chloro-, hydrochloride (1:1);2-(5-Chloro-1H-indol-3-yl)ethanamine hydrochloride (1:1);5-Chloro-1H-indole-3-ethylamine hydrochloride;5-Chloro-1H-indole-3-ethylamine monohydrochloride;

4.What is the molecular formula of 2-(5-Chloro-1H-indol-3-yl)ethanamine hydrochloride?

The chemical formula of ?2-(5-Chloro-1H-indol-3-yl)ethanamine hydrochloride is?C10H12Cl2N2 which containing 10 Carbon atoms,12 Hydrogen atoms,2 Chlorine atoms and 2 Nitrogen atoms,and the molecular weight of??2-(5-Chloro-1H-indol-3-yl)ethanamine hydrochloride?is 231.125.

5.What is 2-(5-Chloro-1H-indol-3-yl)ethanamine hydrochloride (942-26-7) used for?

2-(5-Chloro-1H-indol-3-yl)ethanamine hydrochloride is a chemical compound characterized by a chlorinated indole ring connected to an ethylamine group. It is recognized for its stability in the hydrochloride salt form, which makes it suitable for laboratory applications and research. 2-(5-Chloro-1H-indol-3-yl)ethanamine hydrochloride may exhibit a range of biological activities and interactions with receptors and enzymes, indicating its potential in various pharmaceutical applications.

InChI:InChI=1/C10H11ClN2/c11-8-1-2-10-9(5-8)7(3-4-12)6-13-10/h1-2,5-6,13H,3-4,12H2/p+1

Relevant articles related to 2-(5-Chloro-1H-indol-3-yl)ethanamine hydrochloride:

Article

Source

N6-Substituted Adenosine Receptor Agonists. Synthesis and Pharmacological Activity as Potent Antinociceptive Agents

Guengoer, Timur,Malabre, Patrice,Teulon, Jean-Marie,Camborde, Francoise,Meignen, Joelle,et al.

, p. 4307 - 4316 (2007/10/02)

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