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3-ethyl-2-methyl-7-nitro-1H-indole is a complex organic chemical compound with the molecular formula C12H12N2O2. It is a derivative of indole, a heterocyclic aromatic organic compound that contains a benzene ring fused to a pyrrole ring. The compound is characterized by the presence of an ethyl group at the 3-position, a methyl group at the 2-position, and a nitro group at the 7-position. This specific arrangement of functional groups gives the molecule unique chemical and physical properties, making it a potential candidate for various applications in the fields of pharmaceuticals, agrochemicals, and materials science. Due to its structural complexity, 3-ethyl-2-methyl-7-nitro-1H-indole may exhibit specific reactivity and stability, which can be further explored for its potential uses and interactions with other molecules.

7595-71-3

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7595-71-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7595-71-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,5,9 and 5 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 7595-71:
(6*7)+(5*5)+(4*9)+(3*5)+(2*7)+(1*1)=133
133 % 10 = 3
So 7595-71-3 is a valid CAS Registry Number.

7595-71-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-ethyl-2-methyl-7-nitro-1H-indole

1.2 Other means of identification

Product number -
Other names 2-methyl-3-ethyl-7-nitroindole

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:7595-71-3 SDS

7595-71-3Relevant academic research and scientific papers

2,3-Dialkyl(dimethylamino)indoles: Interaction with 5HT1, 5HT2, and rat stomach fundal serotonin receptors

Fludzinski,Wittenauer,Schenck,Cohen

, p. 2415 - 2418 (2007/10/02)

2,3-Dialkyl(dimethylamino)indoles, synthesized via the Fisher indole synthesis, were found to weakly bind to 5HT1 and 5HT2 sites in brain cortical membranes (IC50 greater than 1 μM at both sites for all compounds). These (dimethylamino)indoles were relatively potent antagonists of the serotonin receptor in the rat stomach fundus. At higher concentrations, several of the compounds were weak agonists at this receptor. For direct comparison with data obtained in the isolated rat fundus, antagonism of serotonin-induced contractions at 5HT2 receptors in the rat jugular vein was also examined. Several of the compounds showed good selectivity for the fundus receptor relative to the 5HT2 receptor; together with minimal affinity for 5HT1 and 5HT2 binding sites in brain cortical membranes, these results support the idea that the serotonin receptor in the stomach fundus is distinct from 5HT1 and 5HT2 binding sites.

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