- Chemical Name 2,2,2-trifluoro-N-(4-mercaptophenyl)acetamide
- CAS No. 94006-35-6
- Contact Us Inquiry
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1.What is the 2,2,2-trifluoro-N-(4-mercaptophenyl)acetamide ?
2,2,2-Trifluoro-N-(4-mercaptophenyl)acetamide is a chemical compound that belongs to the class of acetamides. It is a white crystalline solid with a trifluoromethyl group and a mercaptophenyl group attached to the acetamide functional group, which imparts it with unique properties and applications. 2,2,2-trifluoro-N-(4-mercaptophenyl)acetamide is commonly used as a reagent in organic synthesis and pharmaceutical research, and is known for its ability to act as a selective inhibitor of certain enzymes. It has potential uses in the development of new drugs. However, it is important to handle this chemical with caution as it is considered hazardous and should only be used by trained professionals in a controlled laboratory environment.
2.What is the CAS number for 2,2,2-trifluoro-N-(4-mercaptophenyl)acetamide ?
The CAS number of 2,2,2-trifluoro-N-(4-mercaptophenyl)acetamide is 94006-35-6.
3.What are another words for 2,2,2-trifluoro-N-(4-mercaptophenyl)acetamide ?
Synonyms?for?2,2,2-trifluoro-N-(4-mercaptophenyl)acetamide 94006-35-6:4-(Trifluoroacetylamino)benzenethiol
4.What is 2,2,2-trifluoro-N-(4-mercaptophenyl)acetamide (94006-35-6) used for?
Used in Organic Synthesis:
2,2,2-Trifluoro-N-(4-mercaptophenyl)acetamide is used as a reagent for various organic synthesis processes. Its unique structure allows it to participate in a range of chemical reactions, making it a valuable tool in the synthesis of complex organic molecules.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 2,2,2-trifluoro-N-(4-mercaptophenyl)acetamide is used as a research compound. Its ability to act as a selective inhibitor of certain enzymes makes it a promising candidate for the development of new drugs, particularly those targeting specific biological pathways.
Used in Enzyme Inhibition Studies:
2,2,2-Trifluoro-N-(4-mercaptophenyl)acetamide is used as a selective inhibitor in enzyme inhibition studies. Its interaction with specific enzymes can provide valuable insights into enzyme function and regulation, which can be crucial for understanding disease mechanisms and developing targeted therapeutics.
Used in Controlled Laboratory Environments:
Due to its hazardous nature, 2,2,2-trifluoro-N-(4-mercaptophenyl)acetamide is used exclusively by trained professionals in controlled laboratory environments. Its use is carefully regulated to ensure safety and minimize the risk of adverse effects.
InChI:InChI=1/C8H6F3NOS/c9-8(10,11)7(13)12-5-1-3-6(14)4-2-5/h1-4,14H,(H,12,13)
Relevant articles related to 2,2,2-trifluoro-N-(4-mercaptophenyl)acetamide:
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