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180623-89-6

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180623-89-6 Usage

Description

5-Bromo-7-chloro-1H-indole, a heterocyclic compound with the molecular formula C8H5BrClN, features a 5-bromo-7-chloroindole ring system. It is widely recognized for its potential biological activity and diverse pharmacological properties, such as antifungal, antitumor, and anti-inflammatory activities. This makes it a promising candidate for drug development and a valuable building block in the synthesis of indole-based derivatives for medicinal chemistry and drug discovery.

Uses

Used in Pharmaceutical Research:
5-Bromo-7-chloro-1H-indole is used as a research compound for its potential biological activity, particularly in the development of new drugs with antifungal, antitumor, and anti-inflammatory properties. Its diverse pharmacological effects make it a valuable asset in the discovery and design of novel therapeutic agents.
Used in Agrochemical Research:
In the agrochemical industry, 5-Bromo-7-chloro-1H-indole is utilized as a research compound to explore its potential applications in pest control and crop protection. Its biological activity may contribute to the development of new agrochemical products with enhanced efficacy and selectivity.
Used as an Intermediate in Synthesis:
5-Bromo-7-chloro-1H-indole serves as an intermediate in the synthesis of various pharmaceutical and agrochemical products. Its unique chemical structure allows for the creation of a wide range of indole-based derivatives, expanding the scope of chemical diversity in drug and agrochemical development.
Used in Medicinal Chemistry:
As a building block in medicinal chemistry, 5-Bromo-7-chloro-1H-indole is employed for the preparation of indole-based derivatives. Its structural features facilitate the design and synthesis of new compounds with potential therapeutic applications, contributing to the advancement of drug discovery.
Used in Drug Discovery:
5-Bromo-7-chloro-1H-indole is a key component in drug discovery efforts, where its diverse pharmacological properties are harnessed to identify and develop new drugs with improved efficacy and safety profiles. Its potential applications in various therapeutic areas make it an important tool in the search for innovative treatments.

Check Digit Verification of cas no

The CAS Registry Mumber 180623-89-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,0,6,2 and 3 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 180623-89:
(8*1)+(7*8)+(6*0)+(5*6)+(4*2)+(3*3)+(2*8)+(1*9)=136
136 % 10 = 6
So 180623-89-6 is a valid CAS Registry Number.
InChI:InChI=1/C8H5BrClN/c9-6-3-5-1-2-11-8(5)7(10)4-6/h1-4,11H

180623-89-6SDS

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 5-Bromo-7-chloro-1H-indole

1.2 Other means of identification

Product number -
Other names 1H-Indole,5-bromo-7-chloro

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:180623-89-6 SDS

180623-89-6Downstream Products

180623-89-6Relevant articles and documents

ORGANIC COMPOUNDS AND ORGANIC ELECTRO LUMINESCENCE DEVICE COMPRISING THE SAME

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Paragraph 0231-0233, (2016/10/08)

The present invention relates to a novel organic compound which can be used as a material for an organic electroluminescent element, and an organic electroluminescent element comprising the compound.

Oxazoline antiproliferative agents

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, (2008/06/13)

Compounds having Formula I are useful for treating cancer. Also disclosed are pharmaceutical compositions comprising compounds of Formula I, and methods of treating cancer in a mammal.

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