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4-Isoxazolecarboxylic acid, 5-(4-fluorophenyl)-3-Methyl-, ethyl is a heterocyclic compound with the molecular formula C13H12FNO3. It is a derivative of isoxazolecarboxylic acid, featuring a five-membered ring structure containing both oxygen and nitrogen. 4-Isoxazolecarboxylic acid, 5-(4-fluorophenyl)-3-Methyl-, ethyl's chemical structure includes a fluorophenyl group, a methyl group, and an ethyl group, indicating potential pharmaceutical or biological activity. Its partially lipophilic nature, due to the ethyl group, suggests that it may dissolve in fat or non-polar solvents. These characteristics make 4-Isoxazolecarboxylic acid, 5-(4-fluorophenyl)-3-Methyl-, ethyl a promising candidate for applications in medicinal chemistry and drug development.

1644-03-7

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1644-03-7 Usage

Uses

Used in Pharmaceutical Industry:
4-Isoxazolecarboxylic acid, 5-(4-fluorophenyl)-3-Methyl-, ethyl is used as a pharmaceutical intermediate for the development of new drugs. Its unique chemical structure, including the fluorophenyl and methyl groups, may contribute to its potential as a bioactive molecule with therapeutic properties.
Used in Medicinal Chemistry Research:
In the field of medicinal chemistry, 4-Isoxazolecarboxylic acid, 5-(4-fluorophenyl)-3-Methyl-, ethyl serves as a valuable compound for studying the structure-activity relationships of heterocyclic compounds. Its presence of a fluorine atom and the ethyl group allows researchers to investigate the impact of these functional groups on the compound's biological activity and pharmacokinetic properties.
Used in Drug Delivery Systems:
4-Isoxazolecarboxylic acid, 5-(4-fluorophenyl)-3-Methyl-, ethyl's lipophilic nature due to the ethyl group makes it a suitable candidate for the development of drug delivery systems. It can be incorporated into various formulations, such as nanoparticles or liposomes, to improve the solubility, bioavailability, and targeted delivery of therapeutic agents.
Used in Chemical Synthesis:
As a derivative of isoxazolecarboxylic acid, 4-Isoxazolecarboxylic acid, 5-(4-fluorophenyl)-3-Methyl-, ethyl can be utilized as a building block in the synthesis of more complex heterocyclic compounds. Its unique structure allows for further functionalization and modification, enabling the creation of novel molecules with potential applications in various industries, including pharmaceuticals, agrochemicals, and materials science.

Check Digit Verification of cas no

The CAS Registry Mumber 1644-03-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,6,4 and 4 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1644-03:
(6*1)+(5*6)+(4*4)+(3*4)+(2*0)+(1*3)=67
67 % 10 = 7
So 1644-03-7 is a valid CAS Registry Number.

1644-03-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-(4-fluoro-phenyl)-3-methyl-isoxazole-4-carboxylic acid ethyl ester

1.2 Other means of identification

Product number -
Other names 3-Methyl-4-aethoxycarbonyl-5-(4-fluor-phenyl)-isoxazol

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 -
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More Details:1644-03-7 SDS

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