Date published: 2026-1-20

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6-Methyl-2-heptyne (CAS 51065-64-6)

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Alternate Names:
Methyl isopentyl acetylene
CAS Number:
51065-64-6
Molecular Weight:
110.20
Molecular Formula:
C8H14
Supplemental Information:
This is classified as a Dangerous Good for transport and may be subject to additional shipping charges.
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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6-Methyl-2-heptyne is a compound that functions as an alkyne in experimental applications. It acts as a substrate in various chemical reactions, participating in processes such as alkyne metathesis and Sonogashira coupling. Its mode of action involves the formation of covalent bonds with other molecules, allowing for the synthesis of complex organic compounds. 6-Methyl-2-heptyne′s role includes its use as a building block for the creation of diverse molecular structures, contributing to the development of new materials and compounds. At the molecular level, 6-Methyl-2-heptyne interacts with other reagents to facilitate the formation of carbon-carbon and carbon-heteroatom bonds, enabling the construction of chemical architectures. Its function as an alkyne allows for the manipulation of molecular structures, making it useful for chemists working on the development of novel compounds.


6-Methyl-2-heptyne (CAS 51065-64-6) References

  1. Heterogeneous Phase Microwave-Assisted Reactions under CO₂ or CO Pressure.  |  Calcio Gaudino, E., et al. 2016. Molecules. 21: 253. PMID: 26927033
  2. Highly Permeable Mixed Matrix Hollow Fiber Membrane as a Latent Route for Hydrogen Purification from Hydrocarbons/Carbon Dioxide.  |  Lin, YT., et al. 2021. Membranes (Basel). 11: PMID: 34832094
  3. Antimicrobial analysis of honey against Staphylococcus aureus isolates from wound, ADMET properties of its bioactive compounds and in-silico evaluation against dihydropteroate synthase.  |  Edet, UO., et al. 2023. BMC Complement Med Ther. 23: 39. PMID: 36747234
  4. Antimicrobial analysis of honey against Staphylococcus aureus isolates from wound, ADMET properties of its bioactive compounds and in-silico evaluation against dihydropteroate synthase  |  Uwem Okon Edet, Elizabeth Nkagafel Mbim, Esu Ezeani, Okoroiwu Uchechi Henshaw, Oju R. Ibor, Ini Ubi Bassey, Edet Effiong Asanga, Ekpo Eyo Antai, Francisca O. Nwaokorie, Bassey Okon Edet, Glory P. Bebia, Curtis Tega, Clement I. Mboto, Ani Nkang & Ada Francesca Nneoyi-Egbe. (2023). BMC Complementary Medicine and Therapies. 23, Article number:: 39.
  5. A Combined DFT/IM-MS Study on the Reaction Mechanism of Cationic Ru(II)-Catalyzed Hydroboration of Alkynes  |  Li-Juan Song†, Ting Wang†, Xinhao Zhang*†Orcid, Lung Wa Chung*‡Orcid, and Yun-Dong Wu*†§. 2017,. ACS Catal. 7, 2,: 1361–1368.
  6. Alkylidenecarbenes from acyclic vinyl bromides and potassium tert-butoxide  |  Joseph Wolinsky, Gregory W. Clark, and Patricia C. Thorstenson. 1976,. J. Org. Chem. 41, 5,: 745–750.
  7. Synthesis and gas permeation properties of poly(dialkylacetylenes) containing isopropyl-terminated side-chains  |  Ingo Pinnau, Zhenjie He, Atsushi Morisato. 1 October 2004,. Journal of Membrane Science. Volume 241, Issue 2,: Pages 363-369.
  8. A highly selective cobalt-catalyzed carbonylative cyclization of internal alkynes with carbon monoxide and organic thiols  |  Yoshihiro Higuchi, Shinya Higashimae, Taichi Tamai, Akiya Ogawa. 30 December 2013,. Tetrahedron. Volume 69, Issue 52,: Pages 11197-11202.

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

6-Methyl-2-heptyne, 5 g

sc-278534
5 g
$61.00