Product Name :
2,5-Dihydrofuran (CAS 1708-29-8)
Synonym :
Application :
CAS:
1708-29-8
Purity:
Molecular Weight:
70.09
Formula :
C4H6O
Physical state:
Liquid
solubility :
Shipping Condition :
Store at room temperature
Melting point:
SMILES:
C1C=CCO1
References:
:An efficient synthesis of 2,5-dihydrofuran-fused bicyclic skeletons via the Pd(II)-catalyzed tandem-cyclization reaction of 1,omega-bisallenols. | Deng, Y., et al. 2009. Org Lett. 11: 1205-8. 1075198-30-9 web PMID: 19216524Synthesis of novel 2, 5-dihydrofuran derivatives and evaluation of their anticancer activity. | Zhang, Y., et al. 2012. Eur J Med Chem. tert-Butyl 4-hydroxybutanoate web 48: 69-80. PMID: 22182926Iron-Catalyzed Cyclization of Alkynols with Diorganyl Diselenides: Synthesis of 2,5-Dihydrofuran, 3,6-Dihydro-2H-pyran, and 2,5-Dihydro-1H-pyrrole Organoselanyl Derivatives. | Casola, KK., et al. 2015. J Org Chem. 80: 7702-12. PMID: 26158240Supported Molybdenum Catalysts for the Deoxydehydration of 1,4-Anhydroerythritol into 2,5-Dihydrofuran. | Sandbrink, L., et al. 2017. ChemSusChem. 10: 1375-1379. PMID: 28165202Isosarcophytoxide Derivatives with a 2,5-Dihydrofuran Moiety from the Soft Coral Sarcophyton cinereum. | Chao, CH., et al. 2023. Molecules. 28: PMID: 36677699Analysis of the proton NMR spectra of 2,5-dihydrofuran, 2,5-dihydrothiophene, and butadiene sulfone | R Lozach, B Braillon – Journal of Magnetic Resonance (1969), 1973 – Elsevier. December 1973,. Journal of Magnetic Resonance (1969). Volume 12, Issue 3,: Pages 244-260.Thermal reactions of cyclic ethers at high temperatures. 4. Pyrolysis of 2,5-dihydrofuran behind reflected shocks | Assa Lifshitz, Menashe Bidani, and Shimon Bidani. 1986,. J. Phys. Chem. 90, 22,: 6011–6014.Low-pressure selective hydroformylation of 2,3- and 2,5-dihydrofuran with a rhodium catalyst. Unexpected influence of the auxiliary ligand tris(o-t-butylphenyl) phosphite | A. Polo, J. Real, C. Claver, S. Castillón and J. C. Bayón. , 1990,. J. Chem. Soc., Chem. Commun. 600-601.Focused Microwave-Assisted Synthesis of 2,5-Dihydrofuran Derivatives as Electron Acceptors for Highly Efficient Nonlinear Optical Chromophores | and S. Liu, M.A. Haller, H. Ma, L.R. Dalton, S.-H. Jang, A.K.-Y. Jen. April, 2003. Advanced Materials. Volume15, Issue7-8: Pages 603-607.Rhodium-Catalyzed Diverse Arylation of 2,5-Dihydrofuran: Controllable Divergent Synthesis via Four Pathways | Junhao Xing, Wanjiang Zhu, Bihai Ye, Tao Lu, Tamio Hayashi*, and Xiaowei Dou*. 2020. ACS Catal. , 10, 5,: 2958–2963.Selective isomerization of 2,5-dihydrofuran to 2,3-dihydrofuran using CO-modified, supported Pd catalysts | JR Monnier, JW Medlin, YJ Kuo – Applied Catalysis A: General, 2000 – Elsevier. 13 March 2000,. Applied Catalysis A: General. Volumes 194–195,: Pages 463-474.Can the nonlinearity of hydrogen bonds B…HX be measured precisely? A method from rotational spectroscopy and its application to 2,5-dihydrofuran…HCl | AC Legon, JC Thorn – Chemical physics letters, 1994 – Elsevier. 16 September 1994,. Chemical Physics Letters. Volume 227, Issues 4–5,: Pages 472-479.Ring-closing metathesis toward the synthesis of 2,5-dihydrofuran and 2,5-dihydropyrrole skeletons from Baylis–Hillman adducts | JM Kim, KY Lee, S Lee, JN Kim – Tetrahedron letters, 2004 – Elsevier. 22 March 2004,. Tetrahedron Letters. Volume 45, Issue 13,: Pages 2805-2808.
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