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6-Fluoro-1H-indole-3-carboxylic acid methyl ester is a chemical compound that belongs to the class of organic compounds known as indoles. It features a distinctive indole core structure, which is a bicyclic structure composed of a six-membered benzene ring fused to a five-membered nitrogen-containing pyrrole ring. 6-Fluoro-1H-indole-3-carboxylic acid methyl ester also includes a methyl ester group, which is a methyl group (-CH3) attached to the carboxylic acid portion of the molecule. The 6-fluoro designation indicates the presence of a fluorine atom attached at the 6th position of the indole structure, contributing to its reactivity and potential use in the synthesis of complex molecular structures.

649550-97-0

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649550-97-0 Usage

Uses

Used in Pharmaceutical Research:
6-Fluoro-1H-indole-3-carboxylic acid methyl ester is used as an intermediate compound for the synthesis of various pharmaceuticals. Its unique structure and reactivity make it a valuable building block in the development of new drugs, particularly those targeting specific biological pathways or receptors.
Used in Chemical Synthesis:
In the field of organic chemistry, 6-Fluoro-1H-indole-3-carboxylic acid methyl ester is used as a key component in the synthesis of complex molecular structures. Its presence in the molecule allows for further functionalization and modification, enabling the creation of a wide range of chemical products with diverse applications.
Used in Material Science:
6-Fluoro-1H-indole-3-carboxylic acid methyl ester is employed as a precursor in the development of novel materials with specific properties. Its incorporation into polymers or other materials can lead to enhanced characteristics, such as improved stability, reactivity, or selectivity, which can be beneficial in various industrial applications.
Used in Research and Development:
6-Fluoro-1H-indole-3-carboxylic acid methyl ester is utilized as a research tool in academic and industrial laboratories. Its unique properties and reactivity make it an interesting subject for studies aimed at understanding the fundamental aspects of chemical reactions, as well as for exploring new applications in various fields.

Check Digit Verification of cas no

The CAS Registry Mumber 649550-97-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,4,9,5,5 and 0 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 649550-97:
(8*6)+(7*4)+(6*9)+(5*5)+(4*5)+(3*0)+(2*9)+(1*7)=200
200 % 10 = 0
So 649550-97-0 is a valid CAS Registry Number.

649550-97-0SDS

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 methyl 6-fluoro-1H-indole-3-carboxylate

1.2 Other means of identification

Product number -
Other names 6-fluoro-3-methoxycarbonyl-1H-indole

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:649550-97-0 SDS

649550-97-0Downstream Products

649550-97-0Relevant academic research and scientific papers

Application of new cryptolepine derivatives in controlling and preventing plant-derived germs

-

Paragraph 0013-0017; 0032-0034, (2019/01/14)

The invention relates to the technical field of natural medicinal chemistry and biopesticide, and discloses application of any one compound of 1a-24a of new cryptolepine derivatives in the preparationof a medicament for controlling or resisting rice blast

Fluoroquinolones from imidoylketenes and iminopropadienones, RN≤C≤C≤C≤O

Fulloon, Belinda E.,Wentrup, Curt

experimental part, p. 115 - 120 (2009/08/15)

3-Fluoro-, 4-fluoro-, and 2,3,4-trifluorophenyliminopropadienones have been generated by flash vacuum thermolysis (FVT) of 5-[(fluoroarylamino) methoxymethylene]-2,2-dimethyldioxan-4,6-dione (Meldrum's acid) derivatives. Their reaction with methanol affor

3-GUANIDINOCARBONYL-1-HETEROARYL-INDOLE DERIVATIVES, PREPARATION PROCESS, THEIR USE AS MEDICAMENTS, AND PHARMACEUTICAL COMPOSITIONS COMPRISING THEM

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Page 45, (2008/06/13)

The present invention relates to 3-guanidinocarbonyl-1-heteroaryl-indole derivatives of the formula (I) in which R1 to R5 and Ar have the meaning stated in the claims. The inventive compounds are suitable for example as antiarrhytmic medicaments with cardioprotective component for infarction prophylaxis and infarction treatment and for the treatment of angina pectoris. They also inhibit in a preventive manner the pathophysiological processes associated with the development of ischemia-induced damage, in particular in the triggering of ischemia-induced cardiac arrhytmias and of heart failure.

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