| Weight | 72.107 g/mol |
|---|---|
| Formula | C4H8O |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 0 |
2,3-Dimethyloxirane (21490-63-1, 3266-23-7)
2,3-epoxybutane · 2,3-epoxybutane, (2R-trans)-isomer · 2,3-epoxybutane, (cis)-isomer
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- Stereospecific formation of 1,2-epoxypropane, 1,2-epoxybutane and 1-chloro-2,3-epoxypropane by alkene-utilizing bacteria (Enzyme and Microbial Technology, 1985)
- Comparison of the reactions of methylmagnesium, methyllithium, and methylcopper reagents with 1,2-epoxybutane and 3,4-epoxy-1-butene (Journal of the American Chemical Society, 1970)
- Preparation and determination of configurationally pure trans-(2S,3S)-2,3-epoxybutane (Journal of Organic Chemistry, 1980)
- Theoretical study of the circular dichroism and VUV spectra of trans-2,3-dimethyloxirane (Chemical Physics, 1994)
- Induction of sister chromatid exchange by 3,4-epoxybutane- 1,2-diol in cultured human lymphocytes of different GSTT1 and GSTM1 genotypes (Mutation Research\/environmental Mutagenesis and Related Subjects, 1996)
- Accurate molecular structures and infrared spectra of trans-2,3-dideuterooxirane, methyloxirane, and trans-2,3-dimethyloxirane (Journal of Chemical Physics, 2014)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - 2,3-epoxybutane
- 2,3-epoxybutane, (2R-trans)-isomer
- 2,3-epoxybutane, (cis)-isomer
- 2,3-epoxybutane, (trans)-isomer
-
SMILESCC1C(O1)C
-
InChIKeyPQXKWPLDPFFDJP-UHFFFAOYSA-N
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