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107-54-0

3,5-Dimethylhex-1-yn-3-ol

Catalog#: AR003JDE  |   CAS#: 107-54-0  |   MDL#: MFCD00008941  |   MF: C8H14O  |   MW: 126.1962

Packsize Purity Price Availability Quantity
25g 98% $4.00 Global Stock Buy Now Add To Cart
100g 98% $12.00 Global Stock Buy Now Add To Cart
500g 98% $51.00 Global Stock Buy Now Add To Cart
1kg 98% $99.00 Global Stock Buy Now Add To Cart
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Catalog Number AR003JDE
Chemical Name 3,5-Dimethylhex-1-yn-3-ol
CAS Number 107-54-0
Molecular Formula C8H14O
Molecular Weight 126.1962
MDL Number MFCD00008941
SMILES CC(CC(C#C)(O)C)C
NSC Number 978

As a professional chemist, I can describe the application of 3,5-Dimethylhex-1-yn-3-ol in chemical synthesis.### Application in Chemical Synthesis:
3,5-Dimethylhex-1-yn-3-ol is a versatile compound widely used in organic synthesis due to its unique properties and reactivity. This compound serves as a valuable building block in the production of various pharmaceuticals, agrochemicals, and fine chemicals. Its acetylene functionality makes it a valuable intermediate in the synthesis of more complex organic molecules.**1. Alkynylation Reactions:** 3,5-Dimethylhex-1-yn-3-ol is often employed in alkynylation reactions, where it acts as a precursor to introduce alkynyl groups into organic molecules. This functional group can participate in various coupling reactions, such as Sonogashira or Glaser coupling, to form carbon-carbon bonds and generate diverse chemical structures.**2. Cycloaddition Reactions:** The triple bond in 3,5-Dimethylhex-1-yn-3-ol can undergo cycloaddition reactions with suitable reactants to form cyclic compounds. This reactivity is crucial in the synthesis of heterocycles and complex organic scaffolds.**3. Cross-Coupling Reactions:** 3,5-Dimethylhex-1-yn-3-ol can participate in cross-coupling reactions with appropriate partners to form new carbon-carbon bonds. This enables the creation of extended carbon frameworks and functionalized organic molecules.In summary, 3,5-Dimethylhex-1-yn-3-ol plays a vital role in chemical synthesis by serving as a key intermediate for the construction of diverse organic compounds through alkynylation, cycloaddition, and cross-coupling reactions. Its versatility and reactivity make it a valuable tool for organic chemists in the development of new materials and bioactive compounds.
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