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3-Fluoro-5-(5-((2-methylthiazol-4-yl)-ethynyl)pyridin-2-yl)benzonitrile is a chemical compound with the molecular formula C19H11FN4S. It is a fluorescent dye characterized by its red wavelength fluorescence, which makes it a valuable tool in biomedical research and drug discovery. 3-Fluoro-5-(5-((2-methylthiazol-4-yl)-ethynyl)pyridin-2-yl)benzonitrile is known for its potential applications in pharmaceutical development and as a means to study protein-protein interactions, showcasing its versatility in the fields of medicine and biology.

935685-90-8

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935685-90-8 Usage

Uses

Used in Biomedical Research:
3-Fluoro-5-(5-((2-methylthiazol-4-yl)-ethynyl)pyridin-2-yl)benzonitrile is used as a fluorescent dye for imaging and tracking biological molecules due to its red wavelength fluorescence. This property is particularly useful in visualizing cellular processes and structures, thereby aiding researchers in gaining insights into various biological phenomena.
Used in Drug Discovery:
In the field of drug discovery, 3-Fluoro-5-(5-((2-methylthiazol-4-yl)-ethynyl)pyridin-2-yl)benzonitrile serves as a valuable tool for studying protein-protein interactions. Its ability to fluorescently label proteins allows for the observation of these interactions, which is crucial in understanding disease mechanisms and developing targeted therapeutics.
Used in Pharmaceutical Development:
3-Fluoro-5-(5-((2-methylthiazol-4-yl)-ethynyl)pyridin-2-yl)benzonitrile is used as a potential candidate in the development of new pharmaceuticals. Its unique chemical structure and fluorescent properties make it a promising starting point for the creation of drugs that can target specific biological pathways.
Used in Antiviral and Anticancer Research:
3-Fluoro-5-(5-((2-methylthiazol-4-yl)-ethynyl)pyridin-2-yl)benzonitrile has been studied for its potential antiviral and anticancer properties. Its application in these areas is based on the possibility of using its fluorescent properties to track the effects of antiviral and anticancer treatments, as well as its potential direct activity against viruses and cancer cells.
Overall, 3-Fluoro-5-(5-((2-methylthiazol-4-yl)-ethynyl)pyridin-2-yl)benzonitrile is a multifaceted chemical compound with a broad spectrum of applications in medicine and biology, ranging from basic research to therapeutic development.

Check Digit Verification of cas no

The CAS Registry Mumber 935685-90-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,3,5,6,8 and 5 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 935685-90:
(8*9)+(7*3)+(6*5)+(5*6)+(4*8)+(3*5)+(2*9)+(1*0)=218
218 % 10 = 8
So 935685-90-8 is a valid CAS Registry Number.

935685-90-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-fluoro-5-[5-[2-(2-methyl-1,3-thiazol-4-yl)ethynyl]pyridin-2-yl]benzonitrile

1.2 Other means of identification

Product number -
Other names 3-Fluoro-5-(5-((2-methylthiazol-4-yl)ethynyl)pyridin-2-yl)benzonitrile

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:935685-90-8 SDS

935685-90-8Downstream Products

935685-90-8Relevant academic research and scientific papers

Thiazolyl mglur5 antagonists and methods for their use

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Page/Page column 9, (2009/08/18)

The identification of a unique series of compounds which possesses special advantages in terms of drug-like properties due to their possessing advantageous properties in terms of potency and/or pharmacokinetic and/or selectivity and/or in vivo receptor occupancy properties. Specifically, the selection of a 1,3-thiazol-2-yl ring member linked by an ethynylene to the 3 position of a pyridyl ring or the 5 position of a pyrimidinyl ring, wherein the ring is substituted with selected substituents, results in a compound having superior drug-like properties. The invention includes pharmaceutically acceptable salt forms of these heterocyclic compounds, in particular chloride salts and trifluoroacetate salts.

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