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3-chloro-4-nitro-1H-indole, a derivative of the heterocyclic aromatic organic compound indole, is a pale yellow crystalline powder with the molecular formula C8H5ClN2O2 and a molecular weight of 194.59 g/mol. It is known for its potential biological and pharmacological activities, including anticancer, antibacterial, and antifungal properties, and has been studied for its potential use in the production of pharmaceuticals and other high-value products. However, it is important to handle 3-chloro-4-nitro-1H-indole with caution, as it may pose hazards to human health and the environment.

208511-07-3

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208511-07-3 Usage

Uses

Used in Pharmaceutical Industry:
3-chloro-4-nitro-1H-indole is used as a chemical intermediate for the synthesis of various pharmaceuticals, leveraging its potential biological and pharmacological activities.
Used in Research Applications:
3-chloro-4-nitro-1H-indole is used as a research compound for studying its potential anticancer, antibacterial, and antifungal properties, contributing to the development of new therapeutic agents.
Used in High-Value Product Production:
3-chloro-4-nitro-1H-indole is used as a key component in the production of high-value products, such as specialty chemicals and materials, due to its unique chemical properties and potential applications.

Check Digit Verification of cas no

The CAS Registry Mumber 208511-07-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,8,5,1 and 1 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 208511-07:
(8*2)+(7*0)+(6*8)+(5*5)+(4*1)+(3*1)+(2*0)+(1*7)=103
103 % 10 = 3
So 208511-07-3 is a valid CAS Registry Number.

208511-07-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-Chloro-4-nitro-1H-indole

1.2 Other means of identification

Product number -
Other names 3-chloro-4-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:208511-07-3 SDS

208511-07-3Downstream Products

208511-07-3Relevant academic research and scientific papers

2-imidazolinylaminoindole compounds useful as alpha-2 adrenoceptor agonists

-

, (2008/06/13)

This invention involves compounds having the following structure: wherein: a) R1 is hydrogen; or alkyl; bond (a) is a single or a double bond; b) R2 and R3 are each independently selected from hydrogen; unsubstituted C1-C3 alkanyl, alkenyl or alkynyl; cycloalkanyl, cycloalkenyl; unsubstituted C1-C3 alkylthio or alkoxy; hydroxy; thio; nitro; cyano; amino; C1-C3 alkylamino or C1-C3 dialkylamino and halo; c) R4, R5 and R6 are each independently selected from hydrogen; unsubstituted C1-C3 alkanyl, alkenyl or alkynyl; cycloalkanyl, cycloalkenyl; unsubstituted C1-C3 alkylthio or alkoxy; hydroxy; thio; nitro; cyano; amino; C1-C3 alkylamino or C1-C3 dialkylamino; halo; and 2-imidazolinylamino; and wherein one and only one of R4, R5 and R6 is 2-imidazolinylamino; d) R7 is selected from hydrogen; unsubstituted C1-C3 alkanyl, alkenyl or alkynyl; cycloalkanyl, cycloalkenyl; unsubstituted C1-C3 alkylthio or alkoxy; hydroxy; thio; nitro; cyano; amino; C1-C3 alkylamino or C1-C3 dialkylamino and halo; e) the compound is not 4-(2-imidazolinylamino)indole; enantiomers, optical isomers, stereoisomers, diastereomers, tautomers, addition salts, biohydrolyzable amides and esters thereof, and pharmaceutical compositions comprising such novel compounds. The invention also relates to the use of such compounds for treating disorders modulated by alpha-2 adrenoceptors.

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