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.

Headquartered in New Jersey, USA, ChemScence is a global leading manufacturer and supplier of building blocks and fine research chemicals. We now have branches in Sweden and India. Our mission is to pave the way for drug discovery by providing the most innovative chemicals with the highest-level quality for a reasonable price.

Our Catalog Products

We deliver an extensive portfolio of products, including Building Blocks,Catalysts&Ligands,Synthetic Reagents,Material Science and ADC Linkers&Protac,.ChemScene now have over 600000 Building Blocks & Intermediates in our catalog and more than 70000 of them are in stock.

For details, please refer to the ChemScene website:https://www.chemscene.com