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5,7-Difluoroindole is a chemical compound with the molecular formula C8H5F2N, belonging to the indole family of heterocyclic aromatic organic compounds. It features a five-membered ring with nitrogen and is distinguished by the presence of two fluorine atoms at the 5th and 7th positions of the indole ring. 5,7-Difluoroindole holds potential in medicinal chemistry and drug development due to its unique properties, making it a valuable building block for synthesizing bioactive molecules and pharmaceuticals. Its chemical structure and reactivity also contribute to its utility in organic synthesis and chemical research.

301856-25-7

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301856-25-7 Usage

Uses

Used in Medicinal Chemistry and Drug Development:
5,7-Difluoroindole is used as a building block for the synthesis of bioactive molecules and pharmaceuticals, leveraging its unique properties to create novel compounds with potential therapeutic uses.
Used in Organic Synthesis and Chemical Research:
5,7-Difluoroindole serves as a useful tool in organic synthesis and chemical research, providing a foundation for the development of new chemical reactions and methodologies.

Check Digit Verification of cas no

The CAS Registry Mumber 301856-25-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,0,1,8,5 and 6 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 301856-25:
(8*3)+(7*0)+(6*1)+(5*8)+(4*5)+(3*6)+(2*2)+(1*5)=117
117 % 10 = 7
So 301856-25-7 is a valid CAS Registry Number.
InChI:InChI=1/C8H5F2N/c9-6-3-5-1-2-11-8(5)7(10)4-6/h1-4,11H

301856-25-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 5,7-difluoro-1H-indole

1.2 Other means of identification

Product number -
Other names 1H-INDOLE,5,7-DIFLUORO

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:301856-25-7 SDS

301856-25-7Upstream product

301856-25-7Downstream Products

301856-25-7Relevant academic research and scientific papers

INHIBITORS OF INFLUENZA VIRUS REPLICATION, APPLICATION METHODS AND USES THEREOF

-

, (2018/03/25)

The invention provides a novel class of compounds as inhibitors of influenza virus replication, preparation methods thereof, pharmaceutical compositions containing these compounds, and uses of these compounds and pharmaceutical compositions thereof in the manufacture of medicaments for treating of influenza.

INHIBITORS OF INFLUENZA VIRUS REPLICATION, APPLICATION METHODS AND USES THEREOF

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, (2018/03/09)

A class of compounds as inhibitors of influenza virus replication, preparation methods thereof, pharmaceutical compositions containing these compounds, and uses of these compounds and pharmaceutical compositions thereof in the treatment of influenza.

Influenza virus replication inhibitor and application thereof

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, (2018/11/22)

The invention provides a type of compounds serving as an influenza virus replication inhibitor, a preparation method of the compounds, a pharmaceutical composition comprising the compounds, and application of the compounds and the pharmaceutical composition thereof in treatment of influenza.

INDOLE AHR INHIBITORS AND USES THEREOF

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, (2018/11/22)

The present invention provides compounds useful as inhibitors of AHR, compositions thereof, and methods of using the same.

4-AMINO-6-(HETEROCYCLIC)PICOLINATES AND 6-amino-2-(HETEROCYCLIC)pyrimidine-4-carboxylates AND THEIR USE AS HERBICIDES

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, (2014/09/29)

4-Amino-6-(heterocyclic)picolinic acids and their derivatives; 6-amino-2-(heterocyclic)pyrimidine-4-carboxylates and their derivatives; and methods of using the same as herbicides.

Gold(III)-catalyzed annulation of 2-alkynylanilines: A mild and efficient synthesis of indoles and 3-haloindoles

Arcadi, Antonio,Bianchi, Gabriele,Marinelli, Fabio

, p. 610 - 618 (2007/10/03)

Gold(III)-catalyzed annulation of 2-alkynylanilines in EtOH or EtOH-water mixtures at room temperature gives indoles derivatives in good yields. One-flask protocol for the gold-catalyzed conversion of 2-alkynylanilines to 3-bromo and 3-iodoindoles is also reported.

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