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2-Trifluoroacetyl-4-chloro-5-hydroxyaniline is an organic compound characterized by its unique molecular structure, featuring a trifluoroacetyl group, a chloro substituent, and a hydroxyl group attached to an aniline backbone. It is a yellow solid with potential applications in various chemical processes and industries.

1159977-60-2

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1159977-60-2 Usage

Uses

Used in Organic Synthesis:
2-Trifluoroacetyl-4-chloro-5-hydroxyaniline is used as a synthetic intermediate for the production of various organic compounds. Its unique functional groups allow for versatile chemical reactions, making it a valuable building block in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2-Trifluoroacetyl-4-chloro-5-hydroxyaniline is used as a key intermediate in the synthesis of certain drugs. Its presence in the molecular structure can impart specific biological activities, such as antimicrobial, anti-inflammatory, or analgesic properties, depending on the final compound's design.
Used in Agrochemical Industry:
2-Trifluoroacetyl-4-chloro-5-hydroxyaniline is also utilized in the agrochemical sector as a precursor for the development of new pesticides and herbicides. Its chemical properties can contribute to the effectiveness of these products, enhancing crop protection and yield.
Used in Dye and Pigment Industry:
In the dye and pigment industry, 2-Trifluoroacetyl-4-chloro-5-hydroxyaniline is employed as a starting material for the production of various dyes and pigments. Its yellow color and chemical properties can be modified to create a range of hues and shades for use in textiles, plastics, and other applications.
Used in Research and Development:
2-Trifluoroacetyl-4-chloro-5-hydroxyaniline is also used in research and development settings to explore new chemical reactions and investigate the compound's potential applications in various fields. Its unique structure and properties make it an interesting subject for scientific inquiry and innovation.

Check Digit Verification of cas no

The CAS Registry Mumber 1159977-60-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,5,9,9,7 and 7 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1159977-60:
(9*1)+(8*1)+(7*5)+(6*9)+(5*9)+(4*7)+(3*7)+(2*6)+(1*0)=212
212 % 10 = 2
So 1159977-60-2 is a valid CAS Registry Number.

1159977-60-2Downstream Products

1159977-60-2Relevant academic research and scientific papers

Synthesis and biological activities of potential metabolites of the non-nucleoside reverse transcriptase inhibitor efavirenz

Markwalder, Jay A.,Christ, David D.,Mutlib, Abdul,Cordova, Beverly C.,Klabe, Ronald M.,Seitz, Steven P.

, p. 619 - 622 (2001)

Studies on the biotransformation of the clinically important non-nucleoside reverse transcriptase inhibitor efavirenz have shown that oxidation and secondary conjugation are important components of the processing of this molecule in vivo. We have synthesized metabolites of efavirenz to confirm their structure and to evaluate their activity as antivirals.

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