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2,5,6-Trichloro-1H-indole-3-carbaldehyde is a chemical compound characterized by the molecular formula C9H5Cl3NO. It is an organic compound distinguished by a trichloroindole ring system and a carbaldehyde functional group. 2,5,6-TRICHLORO-1H-INDOLE-3-CARBALDEHYDE is notable for its unique structural and chemical properties, which lend it to a variety of applications in chemical and industrial settings.

800400-47-9

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800400-47-9 Usage

Uses

Used in Chemical Synthesis:
2,5,6-Trichloro-1H-indole-3-carbaldehyde is used as a building block for the synthesis of other organic compounds. Its trichloroindole ring system and carbaldehyde functional group provide a versatile platform for the creation of a range of chemical products.
Used in Organic Synthesis as a Reagent:
In the field of organic synthesis, 2,5,6-trichloro-1H-indole-3-carbaldehyde serves as a reagent, facilitating various chemical reactions that are essential for the production of complex organic molecules.
Used in Fluorescent Dye Development:
2,5,6-Trichloro-1H-indole-3-carbaldehyde is used as a fluorescent dye due to its potential biological activity. Its fluorescent properties make it suitable for applications in biochemistry and molecular biology, where it can be used to label and track biomolecules.
Used in Antifungal Applications:
2,5,6-TRICHLORO-1H-INDOLE-3-CARBALDEHYDE has been studied for its potential as an antifungal agent. Its unique chemical structure may contribute to its effectiveness against fungal infections, making it a candidate for further research and development in this area.
Used in Pharmaceutical Development:
2,5,6-Trichloro-1H-indole-3-carbaldehyde is investigated for its potential use in the development of new pharmaceuticals. Its unique structural and chemical properties suggest that it could be a valuable component in the creation of novel drugs.
Used in Agrochemical Development:
Additionally, 2,5,6-TRICHLORO-1H-INDOLE-3-CARBALDEHYDE has been explored for its potential in the development of new agrochemicals. Its properties may offer advantages in the creation of pesticides or other agricultural chemicals, contributing to more effective and targeted crop protection strategies.

Check Digit Verification of cas no

The CAS Registry Mumber 800400-47-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,0,0,4,0 and 0 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 800400-47:
(8*8)+(7*0)+(6*0)+(5*4)+(4*0)+(3*0)+(2*4)+(1*7)=99
99 % 10 = 9
So 800400-47-9 is a valid CAS Registry Number.

800400-47-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,5,6-TRICHLORO-1H-INDOLE-3-CARBALDEHYDE

1.2 Other means of identification

Product number -
Other names 1H-Indole-3-carboxaldehyde,2,5,6-trichloro

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:800400-47-9 SDS

800400-47-9Relevant academic research and scientific papers

Synthesis, antiviral activity, and mode of action of some 3-substituted 2,5,6-trichloroindole 2′- and 5″-deoxyribonucleosides

Williams, John D.,Ptak, Roger G.,Drach, John C.,Townsend, Leroy B.

, p. 5773 - 5782 (2007/10/03)

A series of chlorinated indole nucleosides has been synthesized and tested for activity against human cytomegalovirus (HCMV) and herpes simplex virus type-1 (HSV-1) and for cytotoxicity. The 2′- and 5′-deoxy derivatives of the reported 3-formyl-2,5,6-tric

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