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(2-Trifluoromethoxy-phenyl)-carbamic acid ethyl ester, also known as ethyl 2-(trifluoromethoxy)phenylcarbamate, is an ethyl ester form of a carbamic acid derivative featuring a trifluoromethoxyphenyl group. This chemical compound is distinguished by the unique reactivity and properties conferred by the trifluoromethoxy group, which can enhance the chemical and biological activity of the products in which it is incorporated.

259137-83-2

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259137-83-2 Usage

Uses

Used in Pharmaceutical Synthesis:
(2-Trifluoromethoxy-phenyl)-carbamic acid ethyl ester serves as an intermediate in the synthesis of pharmaceuticals, contributing to the development of new therapeutic agents. Its unique properties make it a valuable component in medicinal chemistry for creating compounds with specific biological activities.
Used in Agrochemical Production:
(2-Trifluoromethoxy-phenyl)-carbamic acid ethyl ester is also utilized as an intermediate in the production of agrochemicals, where it aids in the synthesis of various organic compounds intended for agricultural applications, such as pesticides and herbicides.
Used in Organic Compound Synthesis:
(2-Trifluoromethoxy-phenyl)-carbamic acid ethyl ester is a potential precursor for the synthesis of a range of organic compounds, highlighting its versatility and importance in organic chemistry for creating diverse chemical entities with potential applications across different industries.

Check Digit Verification of cas no

The CAS Registry Mumber 259137-83-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,5,9,1,3 and 7 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 259137-83:
(8*2)+(7*5)+(6*9)+(5*1)+(4*3)+(3*7)+(2*8)+(1*3)=162
162 % 10 = 2
So 259137-83-2 is a valid CAS Registry Number.

259137-83-2Downstream Products

259137-83-2Relevant academic research and scientific papers

INDOLYL-PIPERIDINYL BENZYLAMINES AS BETA-TRYPTASE INHIBITORS

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Page/Page column 17-18, (2011/07/09)

The present invention discloses and claims a series of substituted indolyl-piperidinyl benzylamines of formula (I), wherein R1, R2 and R3 are as described herein. More specifically, the compounds of this invention are inhibitors of β-tryptase and are, therefore, useful as pharmaceutical agents. Additionally, this invention also discloses methods of preparation of substituted indolyl-piperidinyl benzylamines. In one of the embodiments, there is provided the compounds of formula (I) wherein R3 is (II).

SPIROPIPERIDINE BENZYLAMINES AS BETA-TRYPTASE INHIBITORS

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Page/Page column 28, (2011/07/09)

The present invention discloses and claims a series of substituted spiropiperidine benzylamines of formula (I) wherein R is as described herein. More specifically, the compounds of this invention are inhibitors of β-tryptase and are, therefore, useful as

Piperazine derivatives

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, (2008/06/13)

Piperazine derivatives, as well as pharmaceutically acceptable salts, solvates and esters thereof, can be used in the form of pharmaceutical preparations for the treatment or prevention of disorders of the central nervous system, damage to the central ner

Anti-obesity 1,2,3,4,10,10-a-hexahydropy razino [1,2-a] indoles

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, (2008/06/13)

The present invention is directed to 1,2,3,4,10,10a,-hexahydropyrazino[1,2-a] indole derivatives as well as pharmaceutically acceptable salts, solvates and esters thereof, wherein R1 to R8 have the significance given in claim 1 be used in the form of pharmaceutical preparations for the treatment or prevention of disorders of the central nervous system, damage to the central nervous system, cardiovascular disorders, gastrointestinal disorders, diabetes insipidus, obesity and sleep apnea.

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