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50418-68-3

(2S)-2-hexyloxirane

Catalog#: AR01C3NZ  |   CAS#: 50418-68-3  |   MDL#: MFCD00270134  |   MF: C8H16O  |   MW: 128.212

Packsize Purity Price Availability Quantity
50mg 95% $362.00 2-3 weeks Buy Now Add To Cart
100mg 95% $529.00 2-3 weeks Buy Now Add To Cart
250mg 95% $746.00 2-3 weeks Buy Now Add To Cart
500mg 95% $1,158.00 2-3 weeks Buy Now Add To Cart
1g 95% $1,479.00 2-3 weeks Buy Now Add To Cart
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Catalog Number AR01C3NZ
Chemical Name (2S)-2-hexyloxirane
CAS Number 50418-68-3
Molecular Formula C8H16O
Molecular Weight 128.212
MDL Number MFCD00270134
SMILES CCCCCC[C@@H]1OC1

(2S)-2-Hexyloxirane, also known as (2S)-2-hexyl-oxirane or (S)-hex-2-yl epoxide, is a chiral compound commonly used in chemical synthesis due to its versatile reactivity and stereochemical outcomes. This epoxide is particularly valuable in organic chemistry as a building block for the synthesis of various compounds.One key application of (2S)-2-Hexyloxirane is in the formation of chiral building blocks in organic synthesis. The presence of the epoxide functional group in this compound allows for selective ring-opening reactions with nucleophiles, leading to the formation of new carbon-carbon or carbon-oxygen bonds. The stereochemistry of the epoxide moiety plays a crucial role in determining the stereochemical outcome of these reactions, making (2S)-2-Hexyloxirane a valuable tool for controlling the stereochemistry of the products.Additionally, (2S)-2-Hexyloxirane can serve as a precursor for the synthesis of biologically active molecules, pharmaceutical compounds, or other fine chemicals. By incorporating the (2S)-2-Hexyloxirane subunit into the molecular structure, chemists can introduce specific functional groups or chiral centers strategically, ultimately leading to the desired properties or activities of the final product.The reactivity and stereochemical properties of (2S)-2-Hexyloxirane make it a sought-after compound in the realm of organic synthesis, enabling chemists to access diverse chemical structures with high levels of stereocontrol. Its versatility and synthetic utility make it a valuable asset in the toolbox of synthetic chemists seeking to create complex molecules with precision and efficiency.
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