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712-07-2

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712-07-2 Usage

General Description

The chemical compound "1-(5-chloro-1H-indol-3-yl)propan-2-amine" is an organic compound that belongs to the class of aromatic amine derivatives. It is composed of an indole ring substituted with a chlorine atom at the 5-position and a propan-2-amine group. 1-(5-chloro-1H-indol-3-yl)propan-2-amine may have potential pharmacological properties due to its structural features, and it could be used in various research and development processes for pharmaceuticals or other applications. Its chemical structure and properties make it a subject of interest in the scientific and medical communities for further investigation and exploration.

Check Digit Verification of cas no

The CAS Registry Mumber 712-07-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,1 and 2 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 712-07:
(5*7)+(4*1)+(3*2)+(2*0)+(1*7)=52
52 % 10 = 2
So 712-07-2 is a valid CAS Registry Number.

712-07-2SDS

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-(5-chloro-1H-indol-3-yl)propan-2-amine

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 -
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More Details:712-07-2 SDS

712-07-2Downstream Products

712-07-2Relevant articles and documents

Alpha-ethyltryptamines as dual dopamine-serotonin releasers

Blough, Bruce E.,Landavazo, Antonio,Partilla, John S.,Decker, Ann M.,Page, Kevin M.,Baumann, Michael H.,Rothman, Richard B.

, p. 4754 - 4758 (2015/01/09)

The dopamine (DA), serotonin (5-HT), and norepinephrine (NE) transporter releasing activity and serotonin-2A (5-HT2A) receptor agonist activity of a series of substituted tryptamines are reported. Three compounds, 7b, (+)-7d and 7f, were found to be potent dual DA/5-HT releasers and were >10-fold less potent as NE releasers. Additionally, these compounds had different activity profiles at the 5-HT2Areceptor. The unique combination of dual DA/5-HT releasing activity and 5-HT2Areceptor activity suggests that these compounds could represent a new class of neurotransmitter releasers with therapeutic potential.

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