2-(phenylsulfanyl)-5-(trifluoromethyl)benzenecarbonitrile

≥90%

Reagent Code: #227997
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CAS Number 52548-95-5

science Other reagents with same CAS 52548-95-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 279.28 g/mol
Formula C₁₄H₈F₃NS
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MDL Number MFCD00069139
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of compounds with biological activity. Its structure, featuring a phenylsulfanyl group at position 2, a trifluoromethyl at position 5, and a carbonitrile group, supports use in building blocks for heterocyclic compounds, which are common in drug discovery. The presence of nitrile and trifluoromethyl groups enhances its utility in forming diverse chemical bonds, making it valuable in medicinal chemistry research. Also employed in the creation of selective enzyme inhibitors due to its ability to interact with specific active sites.

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inventory 25mg
10-20 days ฿18,930.00

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2-(phenylsulfanyl)-5-(trifluoromethyl)benzenecarbonitrile
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Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of compounds with biological activity. Its structure, featuring a phenylsulfanyl group at position 2, a trifluoromethyl at position 5, and a carbonitrile group, supports use in building blocks for heterocyclic compounds, which are common in drug discovery. The presence of nitrile and trifluoromethyl groups enhances its utility in forming diverse chemical bonds, making it valuable in medicinal ch

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of compounds with biological activity. Its structure, featuring a phenylsulfanyl group at position 2, a trifluoromethyl at position 5, and a carbonitrile group, supports use in building blocks for heterocyclic compounds, which are common in drug discovery. The presence of nitrile and trifluoromethyl groups enhances its utility in forming diverse chemical bonds, making it valuable in medicinal chemistry research. Also employed in the creation of selective enzyme inhibitors due to its ability to interact with specific active sites.

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