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Ethyl 2-fluorothiazole-4-carboxylate is a chemical compound characterized by the molecular formula C8H6FNO2S. It is a derivative of thiazole, a five-membered heterocyclic compound that includes sulfur and nitrogen atoms. The presence of an ethyl ester group in its structure endows it with lipophilic properties, which are advantageous for organic synthesis and pharmaceutical research. The incorporation of a fluorine atom on the thiazole ring may introduce unique reactivity and properties, making Ethyl 2-fluorothiazole-4-carboxylate a promising candidate for applications in medicinal chemistry and drug discovery due to its structural features and potential biological activity.

153027-86-2

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153027-86-2 Usage

Uses

Used in Pharmaceutical Research:
Ethyl 2-fluorothiazole-4-carboxylate is used as a building block in the synthesis of various pharmaceutical compounds for its ability to enhance the lipophilicity and reactivity of the molecules, which can improve their pharmacokinetic and pharmacodynamic properties.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, Ethyl 2-fluorothiazole-4-carboxylate is utilized as a key intermediate in the development of new drugs, particularly those targeting specific biological pathways or receptors. Its unique structural features, including the fluorine atom, can contribute to the optimization of drug candidates for improved efficacy and selectivity.
Used in Drug Discovery:
Ethyl 2-fluorothiazole-4-carboxylate is employed as a starting material in drug discovery processes, where its structural attributes can be leveraged to design and synthesize novel therapeutic agents with potential applications in treating various diseases and conditions.
Used in Organic Synthesis:
In the realm of organic synthesis, Ethyl 2-fluorothiazole-4-carboxylate is used as a versatile reagent for the preparation of a wide range of organic compounds, taking advantage of its lipophilic nature and the reactivity introduced by the fluorine atom.
Used in Chemical Research:
Ethyl 2-fluorothiazole-4-carboxylate serves as a subject of study in chemical research, where its properties and reactivity are investigated to understand its potential applications and to develop new synthetic methodologies or reaction mechanisms involving this class of compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 153027-86-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,3,0,2 and 7 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 153027-86:
(8*1)+(7*5)+(6*3)+(5*0)+(4*2)+(3*7)+(2*8)+(1*6)=112
112 % 10 = 2
So 153027-86-2 is a valid CAS Registry Number.

153027-86-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name Ethyl 2-fluoro-1,3-thiazole-4-carboxylate

1.2 Other means of identification

Product number -
Other names Ethyl 2-fluorothiazole-4-carboxylate

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:153027-86-2 SDS

153027-86-2Downstream Products

153027-86-2Relevant academic research and scientific papers

Pyrethrinoid esters of thiazole alcohols

-

, (2008/06/13)

In all possible stereoisomer forms and mixtures thereof of the formula STR1 wherein one of R1, R2 or R3 is: STR2

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