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2-Chloro-7-trifluoromethylquinoxaline is a chlorinated derivative of quinoxaline with the molecular formula C8H3ClF3N2, featuring a trifluoromethyl group. This organic compound is recognized for its potential applications in the synthesis of pharmaceuticals and agrochemicals, as well as its use as a reagent in organic synthesis for preparing various quinoxaline derivatives. Its biological activities and pharmacological properties have also garnered interest in the field of medicinal chemistry research.

883-94-3

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883-94-3 Usage

Uses

Used in Pharmaceutical Industry:
2-Chloro-7-trifluoromethylquinoxaline is used as a building block for the synthesis of various pharmaceutical products due to its unique chemical structure and reactivity. Its incorporation into drug molecules can potentially enhance their therapeutic effects and pharmacological properties.
Used in Agrochemical Industry:
In the agrochemical industry, 2-Chloro-7-trifluoromethylquinoxaline serves as a key component in the development of new pesticides. Its chemical properties allow for the creation of compounds with improved efficacy and selectivity against target pests, contributing to more effective and environmentally friendly crop protection solutions.
Used in Organic Synthesis:
2-Chloro-7-trifluoromethylquinoxaline is utilized as a reagent in organic synthesis for the preparation of a variety of quinoxaline derivatives. These derivatives can be further modified or used as intermediates in the synthesis of more complex organic compounds, expanding the scope of chemical research and development.
Used in Medicinal Chemistry Research:
The potential biological activities and pharmacological properties of 2-Chloro-7-trifluoromethylquinoxaline make it a subject of interest in medicinal chemistry research. Its study can lead to the discovery of new therapeutic agents or provide insights into the structure-activity relationships of quinoxaline-based compounds, advancing the understanding of their mechanisms of action and potential applications in medicine.

Check Digit Verification of cas no

The CAS Registry Mumber 883-94-3 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 8,8 and 3 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 883-94:
(5*8)+(4*8)+(3*3)+(2*9)+(1*4)=103
103 % 10 = 3
So 883-94-3 is a valid CAS Registry Number.
InChI:InChI=1/C9H4ClF3N2/c10-8-4-14-6-2-1-5(9(11,12)13)3-7(6)15-8/h1-4H

883-94-3Upstream product

883-94-3Relevant academic research and scientific papers

HETEROARYL DERIVATIVES AS OREXIN RECEPTOR ANTAGONISTS

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Page/Page column 56, (2009/07/10)

The present invention relates to compounds of formula wherein Ar, Het, R1 and n are as defined herein and to pharmaceutically suitable acid addition salts, optically pure enantiomers, racemates or diastereomeric mixtures thereof. Compounds of formula I are orexin receptor antagonists and are useful in the treatment of sleep apnea, narcolepsy, insomnia, parasomnia, jet lag syndrome, circadian rhythms disorder and sleep disorders associated with neurological diseases.

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