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Ethyl 2-fluoro-6-methylbenzoate is a fluoro-substituted aromatic chemical compound with the molecular formula C10H11FO2. It features a methyl group and an ester functional group, which contribute to its unique chemical structure and properties. Ethyl 2-fluoro-6-Methylbenzoate is known for its potential applications in various fields, particularly in the synthesis of pharmaceuticals and organic compounds, as well as in the flavoring of food and cosmetic products.

90259-30-6

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90259-30-6 Usage

Uses

Used in Pharmaceutical Synthesis:
Ethyl 2-fluoro-6-methylbenzoate is used as a key intermediate in the synthesis of various pharmaceuticals and organic compounds. Its unique chemical structure and functional groups make it a valuable building block for the development of new drugs and medicinal agents.
Used in Flavoring Agents:
Ethyl 2-fluoro-6-methylbenzoate is used as a flavoring agent in food and cosmetic products. Its aromatic properties contribute to the development of unique and appealing flavors and scents, enhancing the sensory experience of these products.
Used in Medicinal Chemistry and Drug Development:
Due to its unique chemical structure and functional groups, Ethyl 2-fluoro-6-methylbenzoate may have potential applications in the field of medicinal chemistry and drug development. Researchers can explore its properties and reactivity to design and synthesize novel compounds with therapeutic potential.
Used in Chemical Research:
Ethyl 2-fluoro-6-methylbenzoate can be used as a model compound in chemical research to study the effects of fluorination and methylation on the properties and reactivity of aromatic compounds. This can provide valuable insights into the design and synthesis of new organic compounds and materials.
However, it is important to note that Ethyl 2-fluoro-6-methylbenzoate should be handled and used with caution due to its potential hazards and toxicity. Proper safety measures and guidelines should be followed to minimize risks and ensure the safe application of Ethyl 2-fluoro-6-Methylbenzoate in various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 90259-30-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,2,5 and 9 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 90259-30:
(7*9)+(6*0)+(5*2)+(4*5)+(3*9)+(2*3)+(1*0)=126
126 % 10 = 6
So 90259-30-6 is a valid CAS Registry Number.

90259-30-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 2-fluoro-6-methylbenzoate

1.2 Other means of identification

Product number -
Other names Benzoic acid,2-fluoro-6-methyl-,ethyl ester

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:90259-30-6 SDS

90259-30-6Downstream Products

90259-30-6Relevant academic research and scientific papers

INFLUENZA VIRUS REPLICATION INHIBITOR AND USES THEREOF

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Paragraph 00190; 00306-00307, (2020/05/21)

The invention belongs to the field of medicine, and particularly relates to a novel compound as a replication inhibitor of influenza virus and a preparation method thereof, a pharmaceutical composition comprising the compound and use of the compound and pharmaceutical composition thereof in treating influenza. The present invention provides a compound having Formula (I) or a stereoisomer, a tautomer, an N-oxide, a solvate, a metabolite, a pharmaceutically acceptable salt or a prodrug thereof, The compound of the present invention can inhibit influenza virus well, and/or has lower cytotoxicity, better in vivo pharmacokinetic properties and in vivo pharmacodynamic properties.

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