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61668-02-8

1-(4-Fluorophenyl)but-3-en-1-one

Catalog#: AR01AK5O  |   CAS#: 61668-02-8  |   MDL#: MFCD14653094  |   MF: C10H9FO  |   MW: 164.1763

Packsize Purity Price Availability Quantity
50mg 95% $211.00 2-3 weeks Buy Now Add To Cart
100mg 95% $303.00 2-3 weeks Buy Now Add To Cart
250mg 95% $423.00 2-3 weeks Buy Now Add To Cart
500mg 95% $685.00 2-3 weeks Buy Now Add To Cart
1g 95% $870.00 2-3 weeks Buy Now Add To Cart
2.5g 95% $1,678.00 2-3 weeks Buy Now Add To Cart
5g 95% $2,472.00 2-3 weeks Buy Now Add To Cart
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Catalog Number AR01AK5O
Chemical Name 1-(4-Fluorophenyl)but-3-en-1-one
CAS Number 61668-02-8
Molecular Formula C10H9FO
Molecular Weight 164.1763
MDL Number MFCD14653094
SMILES C=CCC(=O)c1ccc(cc1)F

1-(4-Fluorophenyl)but-3-en-1-one, also known as $name$, is a versatile compound commonly used in chemical synthesis processes. Due to its unique molecular structure, this compound serves as a valuable building block in the synthesis of various organic compounds.In organic chemistry, $name$ is utilized as a key intermediate in the production of pharmaceuticals, agrochemicals, and specialty chemicals. Its conjugated double bonds and substituted phenyl group provide opportunities for functional group transformations, making it a valuable precursor in the preparation of complex molecules.One of the key applications of $name$ in chemical synthesis is its role as a starting material for the synthesis of chalcone derivatives. Chalcones are a class of compounds with diverse biological activities, including antioxidant, anti-inflammatory, and anticancer properties. By reacting $name$ with appropriate reagents, chemists can efficiently access various chalcone derivatives for further biological evaluation.Additionally, $name$ can undergo reactions such as nucleophilic additions, condensations, and reductions to introduce different functional groups into the molecule, expanding its synthetic utility. This compound's reactivity and versatility make it a valuable tool for organic chemists seeking to construct complex molecular frameworks efficiently and with high precision.
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