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65939-59-5

1-Hepten-6-yne

Catalog#: AR00FCLG  |   CAS#: 65939-59-5  |   MDL#: MFCD00190232  |   MF: C7H10  |   MW: 94.1543

Packsize Purity Price Availability Quantity
50mg 95% $276.00 2-3 weeks Buy Now Add To Cart
100mg 95% $399.00 2-3 weeks Buy Now Add To Cart
250mg 95% $560.00 2-3 weeks Buy Now Add To Cart
500mg 95% $868.00 2-3 weeks Buy Now Add To Cart
1g 95% $1,105.00 2-3 weeks Buy Now Add To Cart
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Catalog Number AR00FCLG
Chemical Name 1-Hepten-6-yne
CAS Number 65939-59-5
Molecular Formula C7H10
Molecular Weight 94.1543
MDL Number MFCD00190232
SMILES C=CCCCC#C

1-Hepten-6-yne, also known as 6-heptyne, is a versatile compound widely used in chemical synthesis processes. In organic chemistry, 1-Hepten-6-yne serves as a valuable building block for the synthesis of various important compounds. Its terminal alkyne functional group allows for diverse reactions, making it a key intermediate in the preparation of complex organic molecules. One of the notable applications of 1-Hepten-6-yne is in the synthesis of heterocycles and pharmaceuticals. By undergoing various functional group transformations, such as addition reactions and cross-coupling reactions, 1-Hepten-6-yne can be utilized to create structurally diverse compounds with potential biological activities. Its ability to participate in Sonogashira coupling, Glaser coupling, and related reactions further expands its utility in the synthesis of functionalized organic molecules.Moreover, 1-Hepten-6-yne serves as a useful reagent in the preparation of conjugated systems and π-extended molecules. Its unique chemical structure allows for the formation of conjugated diynes and polyynes, which are important for the development of materials with interesting electronic and optical properties. Additionally, the presence of the alkyne moiety in 1-Hepten-6-yne enables its utilization in the construction of molecular frameworks for supramolecular chemistry studies.Overall, the versatility of 1-Hepten-6-yne in chemical synthesis makes it a valuable tool for organic chemists seeking to access novel compounds and functionalized materials through strategic bond-forming reactions.
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