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171032-87-4

(S)-1-(2-Fluorophenyl)ethanol

Catalog#: AR007UY6  |   CAS#: 171032-87-4  |   MDL#: MFCD03092992  |   MF: C8H9FO  |   MW: 140.1549

Packsize Purity Price Availability Quantity
25mg 97% $5.00 Global Stock Buy Now Add To Cart
100mg 97% $7.00 Global Stock Buy Now Add To Cart
250mg 97% $13.00 Global Stock Buy Now Add To Cart
500mg 97% $23.00 Global Stock Buy Now Add To Cart
1g 97% $42.00 Global Stock Buy Now Add To Cart
5g 97% $154.00 Global Stock Buy Now Add To Cart
10g 97% $183.00 Global Stock Buy Now Add To Cart
25g 97% $366.00 Global Stock Buy Now Add To Cart
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Catalog Number AR007UY6
Chemical Name (S)-1-(2-Fluorophenyl)ethanol
CAS Number 171032-87-4
Molecular Formula C8H9FO
Molecular Weight 140.1549
MDL Number MFCD03092992
SMILES C[C@@H](c1ccccc1F)O

(S)-1-(2-Fluorophenyl)ethanol, also known as (S)-2-fluorophenylethanol, is a versatile compound widely used in chemical synthesis. This chiral alcohol plays a crucial role in asymmetric synthesis, where it serves as a valuable building block for the preparation of various pharmaceuticals, agrochemicals, and fine chemicals.One of the key applications of (S)-1-(2-Fluorophenyl)ethanol is in the synthesis of chiral molecules. Due to its chiral nature, this compound can be employed as a chiral auxiliary or a chiral ligand in asymmetric reactions, enabling the creation of enantiomerically pure compounds. Its distinct stereochemistry makes it a valuable tool in the production of optically active substances with high enantiomeric purity.Additionally, (S)-1-(2-Fluorophenyl)ethanol can be utilized in the synthesis of fluorinated organic compounds. The presence of the fluorine atom in its structure imparts unique properties to the resulting molecules, making them desirable in pharmaceutical and material science applications. This compound can participate in various transformations, such as Grignard reactions, oxidation reactions, and acylation reactions, leading to the formation of diverse fluorinated compounds.Furthermore, (S)-1-(2-Fluorophenyl)ethanol finds applications in the preparation of fragrance and flavor compounds. Its aromatic moiety, combined with the fluorine substituent, contributes to the development of novel scent and taste molecules. By incorporating this compound into the synthesis of fragrance ingredients, it is possible to achieve complex and intriguing olfactory profiles that appeal to discerning consumers.In conclusion, (S)-1-(2-Fluorophenyl)ethanol is a valuable compound in chemical synthesis, offering opportunities for the creation of enantiomerically pure compounds, fluorinated organic molecules, and fragrance ingredients. Its versatility and unique structural features make it a sought-after reagent in the field of organic chemistry, enabling the development of diverse and functionalized compounds for various industrial applications.
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