Molecular structure of 3-Butyn-2-ol, CAS Number: 2028-63-9
3-Butyn-2-ol (CAS 2028-63-9)
CAS Number:
2028-63-9
Molecular Weight:
70.09
Molecular Formula:
C4H6O
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.
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SDS & Certificate of Analysis
3-Butyn-2-ol is a clear, colorless, and viscous liquid that possesses a characteristic smell. It is soluble in water, ethanol, and ether. 3-Butyn-2-ol has multiple applications in scientific experiments, including organic synthesis, catalysis, and materials science. For example, it is used as a starting material for the synthesis of different organic compounds, such as ethynyl compounds and vinyl ethers. Furthermore, 3-Butyn-2-ol is used as a catalyst in different chemical reactions, such as Sonogashira coupling and hydroamination, due to its triple bond.
3-Butyn-2-ol (CAS 2028-63-9) References
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- Solid-phase synthesis of 5-isoxazol-4-yl-[1,2,4]oxadiazoles. | Quan, C. and Kurth, M. 2004. J Org Chem. 69: 1470-4. PMID: 14986998
- Application of a (1)H delta-resolved 2D NMR experiment to the visualization of enantiomers in chiral environment, using sample spatial encoding and selective echoes. | Giraud, N., et al. 2009. Magn Reson Chem. 47: 300-6. PMID: 19152377
- Determination of volatile organic compounds in exhaled breath of patients with lung cancer using solid phase microextraction and gas chromatography mass spectrometry. | Ligor, M., et al. 2009. Clin Chem Lab Med. 47: 550-60. PMID: 19397483
- Highly enantioselective reduction of 4-(trimethylsilyl)-3-butyn-2-one to enantiopure (R)-4-(trimethylsilyl)-3-butyn-2-ol using a novel strain Acetobacter sp. CCTCC M209061. | Xiao, ZJ., et al. 2009. Bioresour Technol. 100: 5560-5. PMID: 19564106
- Protective group-free syntheses of (±)-frontalin, (±)-endo-brevicomin, (±)-exo-brevicomin, and (±)-3,4-dehydro-exo-brevicomin: racemic pheromones with a 6,8-dioxabicyclo[3.2.1]octane ring. | Mori, K. 2011. Biosci Biotechnol Biochem. 75: 976-81. PMID: 21597189
- Matrix isolation-vibrational circular dichroism spectroscopy of 3-butyn-2-ol and its binary aggregates. | Merten, C. and Xu, Y. 2013. Chemphyschem. 14: 213-9. PMID: 23109050
- Synthesis and cytotoxicity on human leukemia cells of furonaphthoquinones isolated from tabebuia plants. | Inagaki, R., et al. 2013. Chem Pharm Bull (Tokyo). 61: 670-3. PMID: 23727782
- Reactivity of Cl atom with triple-bonded molecules. An experimental and theoretical study with alcohols. | Alwe, HD., et al. 2014. J Phys Chem A. 118: 7695-706. PMID: 25146879
- Zn-Promoted Selective Gas-Phase Hydrogenation of Tertiary and Secondary C4 Alkynols over Supported Pd. | González-Fernández, A., et al. 2020. ACS Appl Mater Interfaces. 12: 28158-28168. PMID: 32479052
- Accuracy of quantum chemistry structures of chiral tag complexes and the assignment of absolute configuration. | Mayer, K., et al. 2022. Phys Chem Chem Phys. 24: 27705-27721. PMID: 36374162
- Vibrational Circular Dichroism, Predominant Conformations, and Hydrogen Bonding in (S)-(−)-3-Butyn-2-ol | Feng Wang and Prasad L. Polavarapu. 2000. J. Phys. Chem. A. 104: 1822–1826.
- Gas-Phase Catalytic Hydrogenation/Isomerization in the Transformation of 3-Butyn-2-ol over Pd-Ni/Al2O3 | Alberto González-Fernández, Chiara Pischetola, and Fernando Cárdenas-Lizana*. 2021. J. Phys. Chem. C. 125: 2454–2463.
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
3-Butyn-2-ol, 25 ml | sc-225994 | 25 ml | $63.00 |