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(2-tert-Butoxycarbonylamino-4-trifluoromethyl-phenyl)-oxo-acetic acid ethyl ester is an ester derivative of a carboxylic acid that features a tert-butoxycarbonyl (Boc) protecting group, a trifluoromethyl-substituted phenyl group, and an ethyl ester function. This versatile compound plays a significant role in organic chemistry, particularly as an intermediate in the synthesis of pharmaceuticals and complex molecules.
Used in Pharmaceutical Industry:
(2-tert-Butoxycarbonylamino-4-trifluoromethyl-phenyl)-oxo-acetic acid ethyl ester is used as an intermediate in the synthesis of pharmaceuticals for its ability to facilitate the production of complex molecular structures. The presence of the Boc protecting group allows for selective chemical transformations, enhancing the compound's utility in creating specific drug molecules.
Used in Materials Science:
In the field of materials science, (2-tert-Butoxycarbonylamino-4-trifluoromethyl-phenyl)-oxo-acetic acid ethyl ester may be utilized in the development of new materials, taking advantage of its unique structural features and reactivity. Its potential applications could range from the creation of novel polymers to the development of advanced materials with specific properties.
Used as a Reagent in Chemical Reactions:
(2-tert-Butoxycarbonylamino-4-trifluoromethyl-phenyl)-oxo-acetic acid ethyl ester also serves as a reagent in various chemical reactions, providing a means to achieve specific chemical outcomes. Its role as a reagent can be crucial in the synthesis of a wide array of organic compounds, contributing to the advancement of organic chemistry.

159684-36-3

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159684-36-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 159684-36-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,9,6,8 and 4 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 159684-36:
(8*1)+(7*5)+(6*9)+(5*6)+(4*8)+(3*4)+(2*3)+(1*6)=183
183 % 10 = 3
So 159684-36-3 is a valid CAS Registry Number.

159684-36-3Relevant academic research and scientific papers

Catalytic enantioselective fluorination of oxindoles

Hamashima, Yoshitaka,Suzuki, Toshiaki,Takano, Hisashi,Shimura, Yuta,Sodeoka, Mikiko

, p. 10164 - 10165 (2007/10/03)

We have developed a highly efficient catalytic enantioselective fluorination of oxindole derivatives. In the presence of a catalytic amount of chiral Pd complex 2 (2.5 mol %), various substrates, including aryl- and alkyl-substituted oxindoles, were fluor

A General Method for the Synthesis of Isatins: Preparation of Regiospecifically Functionalized Isatins from Anilines

Hewawasam, Piyasena,Meanwell, Nicholas A.

, p. 7303 - 7306 (2007/10/02)

A new method has been developed for regiospecific conversion of substituted anilines to isatins.The method utilizes the reaction of an ortho-lithiated, protected aniline derivative with diethyl oxalate to furnish an α-ketoester.Hydrolytic deprotection of the amino moiety is accompanied by cyclization to provide the isatin.

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