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1-(4-fluorophenyl)-2,3,4,9-tetrahydro-1H-beta-carboline hydrochloride (1:1) is a complex organic compound with the molecular formula C14H16ClFN2. It is a derivative of beta-carboline, a naturally occurring alkaloid found in various plants and fungi. This specific compound features a 4-fluorophenyl group attached to the beta-carboline core, which may influence its chemical properties and potential applications. The hydrochloride salt form indicates that it is a salt of the parent compound, which can affect its solubility and stability. 1-(4-fluorophenyl)-2,3,4,9-tetrahydro-1H-beta-carboline hydrochloride (1:1) is of interest in the field of medicinal chemistry, potentially for its neuroactive properties or as a research tool in studying the effects of beta-carboline derivatives on biological systems.

3380-82-3

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3380-82-3 Usage

Appearance

White or off-white crystalline powder

Usage

Research and study of neurochemistry and neuroscience

Central Nervous System Effects

Potential effects on the central nervous system

Receptor Affinity

High affinity for serotonin receptors

Mood Regulation

Investigated for its potential role in mood regulation and behavior

Therapeutic Applications

Potential use in treating conditions such as depression and anxiety disorders

Pain Perception

Studied for its potential role in modulating pain perception and tolerance

Laboratory Studies

Commonly used in laboratory settings for research purposes

Check Digit Verification of cas no

The CAS Registry Mumber 3380-82-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,3,8 and 0 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 3380-82:
(6*3)+(5*3)+(4*8)+(3*0)+(2*8)+(1*2)=83
83 % 10 = 3
So 3380-82-3 is a valid CAS Registry Number.

3380-82-3SDS

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 1-(4-fluorophenyl)-2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indole,hydrochloride

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

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

More Details:3380-82-3 SDS

3380-82-3Relevant academic research and scientific papers

Microwave-assisted one-pot preparation of tetrahydro-β-carboline hydrochlorides under solvent-free conditions

Liu, Fei,You, Qi-Dong

, p. 3933 - 3938 (2007)

An efficient and environmentally friendly synthesis of tetrahydro-β- carboline hydrochlorides via Pictet-Spengler reaction was described. Tryptamine hydrochlorides were used as the reactant and no additional acid catalyst was needed. This reaction was com

Asymmetric Biocatalytic Synthesis of 1-Aryltetrahydro-β-carbolines Enabled by “Substrate Walking”

Eger, Elisabeth,Iding, Hans,Kroutil, Wolfgang,Kuhn, Bernd,Schrittwieser, Joerg H.,Wetzl, Dennis

supporting information, p. 16281 - 16285 (2020/11/30)

Stereoselective catalysts for the Pictet–Spengler reaction of tryptamines and aldehydes may allow a simple and fast approach to chiral 1-substituted tetrahydro-β-carbolines. Although biocatalysts have previously been employed for the Pictet–Spengler react

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