1,4-Diphenylbutadiyne (CAS 886-66-8)
QUICK LINKS
1,4-Diphenylbutadiyne (1,4-DPB) is an organic compound. The versatility of 1,4-Diphenylbutadiyne is evident through its wide range of applications, spanning from organic synthesis to nanotechnology. In scientific research, 1,4-Diphenylbutadiyne has found numerous applications. It serves as a valuable precursor in organic synthesis, facilitating the creation of various compounds. Despite its extensive use, the precise mechanism of action of 1,4-Diphenylbutadiyne is yet to be fully comprehended. Researchers speculate that it interacts with proteins and other molecules in diverse ways. These interactions have been observed to activate specific pathways while inhibiting others. Moreover, the compound′s interactions with certain molecules lead to the formation of new compounds or the modification of existing ones.
1,4-Diphenylbutadiyne (CAS 886-66-8) References
- Synthesis and characterization of bis(S-acetylthio)-derivatized europium triple-decker monomers and oligomers. | Schweikart, KH., et al. 2003. Inorg Chem. 42: 7431-46. PMID: 14606839
- Poly(diacetylene)-nanofibers can be fabricated through photo-irradiation using natural polysaccharide schizophyllan as a one-dimensional mold. | Hasegawa, T., et al. 2005. Org Biomol Chem. 3: 4321-8. PMID: 16327892
- Palladacycles of novel bisoxazoline chelating ligands based on the dimeric cyclobutadiene linked cobalt sandwich compound [(η5-Cp)Co(η4-C4Ph3)]2. | Singh, N. and Elias, AJ. 2011. Dalton Trans. 40: 4882-91. PMID: 21416080
- Synthesis of 7,8-dehydropurpurin dimers and their conversion into conformationally constrained β-to-β vinylene-bridged porphyrin dimers. | Fukui, N., et al. 2014. Angew Chem Int Ed Engl. 53: 4395-8. PMID: 24644098
- Plasmonic Switching of the Reaction Pathway: Visible-Light Irradiation Varies the Reactant Concentration at the Solid-Solution Interface of a Gold-Cobalt Catalyst. | Peiris, E., et al. 2019. Angew Chem Int Ed Engl. 58: 12032-12036. PMID: 31095843
- Cooperation in Cu-MOF-74-Derived Cu-Cu2O-C Nanocomposites To Enable Efficient Visible-Light-Initiated Phenylacetylene Coupling. | Cai, J., et al. 2019. Inorg Chem. 58: 7997-8002. PMID: 31185556
- Polymer Nanofibers Exhibiting Remarkable Activity in Driving the Living Polymerization under Visible Light and Reusability. | Xia, L., et al. 2020. Adv Sci (Weinh). 7: 1902451. PMID: 32195082
- Distance-Selected Topochemical Dehydro-Diels-Alder Reaction of 1,4-Diphenylbutadiyne toward Crystalline Graphitic Nanoribbons. | Zhang, P., et al. 2020. J Am Chem Soc. 142: 17662-17669. PMID: 32900188
- Phase Change-Driven Negative Activation Energies in Pd/Carbon-Based/Organic Getter Hydrogenation Reactions. | Dinh, LN., et al. 2020. J Phys Chem A. 124: 8390-8397. PMID: 32966071
- Intense Molar Circular Dichroism in Fully Conjugated All-Carbon Macrocyclic 1,3-Butadiyne Linked pseudo-meta [2.2]Paracyclophanes. | Sidler, E., et al. 2022. Chemistry. 28: e202201764. PMID: 35781897
- Artificial synapse based on 1,4-diphenylbutadiyne with femtojoule energy consumption. | Liu, J., et al. 2023. Phys Chem Chem Phys. 25: 5453-5458. PMID: 36745478
- Catalytic, Z-Selective, Semi-Hydrogenation of Alkynes with a Zinc-Anilide Complex. | Baker, GJ., et al. 2023. J Am Chem Soc. 145: 7667-7674. PMID: 36972405
- 1,4-Diphenylbutadiyne, a new non-photodynamic phototoxic compound. | Kagan, J., et al. 1980. Photochem Photobiol. 32: 607-11. PMID: 7012855
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
1,4-Diphenylbutadiyne, 1 g | sc-223056 | 1 g | $51.00 |