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51748-27-7

3-(TRIFLUOROMETHYLTHIO)BENZALDEHYDE

Catalog#: AR00DD9E  |   CAS#: 51748-27-7  |   MDL#: MFCD00236335  |   MF: C8H5F3OS  |   MW: 206.1849

Packsize Purity Price Availability Quantity
100mg 95% $6.00 Global Stock Buy Now Add To Cart
250mg 95% $10.00 Global Stock Buy Now Add To Cart
1g 95% $22.00 Global Stock Buy Now Add To Cart
5g 95% $101.00 Global Stock Buy Now Add To Cart
10g 95% $201.00 Global Stock Buy Now Add To Cart
25g 95% $380.00 Global Stock Buy Now Add To Cart
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Catalog Number AR00DD9E
Chemical Name 3-(TRIFLUOROMETHYLTHIO)BENZALDEHYDE
CAS Number 51748-27-7
Molecular Formula C8H5F3OS
Molecular Weight 206.1849
MDL Number MFCD00236335
SMILES O=Cc1cccc(c1)SC(F)(F)F

3-((Trifluoromethyl)thio)benzaldehyde, also known as $name$, is a versatile chemical reagent commonly used in organic synthesis. With its unique structure combining a benzaldehyde group with a trifluoromethylthio moiety, this compound offers a wide range of applications in the field of chemistry.One key application of $name$ is its role as a building block in the synthesis of various pharmaceuticals and agrochemicals. The presence of the trifluoromethylthio group imparts desirable properties to the molecules being synthesized, such as improved bioavailability, metabolic stability, and binding affinity. This makes $name$ a valuable tool for medicinal chemists and researchers working on developing new drugs and crop protection agents.Additionally, 3-((Trifluoromethyl)thio)benzaldehyde can also be employed in the preparation of advanced materials and fine chemicals. Its reactive benzaldehyde functionality allows for the selective introduction of the trifluoromethylthio group at specific positions within a molecule, enabling the creation of complex structures with tailored properties. This has applications in the synthesis of optoelectronic materials, functional polymers, and specialty chemicals.Furthermore, $name$ serves as a useful reagent in organic transformations, such as cross-coupling reactions, oxidation processes, and heterocycle synthesis. Its versatile nature and compatibility with a variety of reaction conditions make it a valuable tool for chemists looking to modify or functionalize organic molecules in a controlled manner.
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GHS Pictogram
Signal Word Warning
UN# N/A
Hazard Statements H227-H302-H315-H319-H335
Precautionary Statements P261-P305+P351+P338
Class N/A
Packing Group N/A

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