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53589-56-3

3,3-Dimethylpent-4-En-1-Ol

Catalog#: AR01B65X  |   CAS#: 53589-56-3  |   MDL#: MFCD07780544  |   MF: C7H14O  |   MW: 114.1855

Packsize Purity Price Availability Quantity
50mg 95% $164.00 2-3 weeks Buy Now Add To Cart
100mg 95% $234.00 2-3 weeks Buy Now Add To Cart
250mg 95% $322.00 2-3 weeks Buy Now Add To Cart
500mg 95% $585.00 2-3 weeks Buy Now Add To Cart
1g 95% $751.00 2-3 weeks Buy Now Add To Cart
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Catalog Number AR01B65X
Chemical Name 3,3-Dimethylpent-4-En-1-Ol
CAS Number 53589-56-3
Molecular Formula C7H14O
Molecular Weight 114.1855
MDL Number MFCD07780544
SMILES OCCC(C=C)(C)C

3,3-Dimethylpent-4-en-1-ol, also known as $name$, is a versatile compound widely used in chemical synthesis. Its unique structure and properties make it a valuable reagent in organic chemistry.One important application of $name$ is as a reagent in the synthesis of complex organic molecules. Its double bond and functional group make it useful for creating carbon-carbon bonds through various reactions such as alkene metathesis, hydroboration, and oxidation. This compound is often employed in the construction of pharmaceuticals, agrochemicals, and fine chemicals due to its ability to serve as a building block in the formation of intricate molecular structures.Moreover, $name$ can be utilized in asymmetric synthesis processes to produce enantiomerically pure compounds. By using chiral catalysts or reagents in conjunction with this compound, chemists can control the stereochemistry of the products, enabling the creation of optically active molecules with specific biological activities or properties.In addition to its role in chemical synthesis, $name$ can also act as a ligand in transition metal-catalyzed reactions. Its ability to coordinate with metals such as palladium, ruthenium, or rhodium allows for the formation of stable complexes that facilitate numerous transformations, including cross-coupling reactions and hydrogenation processes.Overall, the diverse applications of 3,3-Dimethylpent-4-en-1-ol make it a valuable tool in the arsenal of synthetic chemists, enabling the efficient construction of complex molecules with tailored properties and stereochemistry.
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