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4-[4-chloro-2-(6-methoxypyridin-2-yl)-7-(trifluoromethyl)-1H-indol-3-yl]butan-1-amine is a complex organic compound with a molecular formula of C22H20ClF3N4O. It is characterized by a 1H-indole-3-yl core, which is substituted with a 4-chloro group, a 6-methoxypyridin-2-yl group, and a trifluoromethyl group. The compound also features a butan-1-amine chain attached to the 4-position of the indole ring. This chemical structure suggests potential applications in pharmaceuticals or as a precursor in the synthesis of other complex molecules, given its diverse functional groups and aromatic systems.

5020-62-2

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5020-62-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5020-62-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,0,2 and 0 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 5020-62:
(6*5)+(5*0)+(4*2)+(3*0)+(2*6)+(1*2)=52
52 % 10 = 2
So 5020-62-2 is a valid CAS Registry Number.

5020-62-2SDS

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 4-[4-chloro-2-(6-methoxypyridin-2-yl)-7-(trifluoromethyl)-1H-indol-3-yl]butan-1-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

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More Details:5020-62-2 SDS

5020-62-2Relevant academic research and scientific papers

SYNTHESIS OF TRICYCLIC BENZAZEPINES AND THEIR DOPAMINE D1- AND D2-AFFINITY

Horn Jensen, Eva,Nielsen, Per Halfdan

, p. 2441 - 2458 (2007/10/03)

A new group of angular 8,9-annelated 3-benzazepines has been found to be potent and selective dopamine D1-receptor antagonists of interest as possible pharmaceuticals in the treatment of schizophrenia.The synthesis of three new conformationally constrained representatives of this group of benzazepines is described and their affinity to the D1-receptor evaluated.Although none of these proved superior to the previously examined compounds, useful information on the receptor binding site was obtained.

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