Weight | 72.107 g/mol |
---|---|
Formula | C4H8O |
Hydrogen Acceptors | 1 |
Hydrogen Donors | 1 |
Aromatic Rings | 0 |
Rotatable Bonds | 1 |
2-Buten-1-ol (6117-91-5)
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- Hydroxyaldehyde products from hydroxyl radical reactions of Z-3-hexen-1-ol and 2-methyl-3-buten-2-ol quantified by SPME and API-MS. (Environmental Science & Technology, 2003)
- Highly stereoselective and general synthesis of (z)-3-methyl-2-alken-1-ols via palladium-catalyzed cross coupling of (z)-3-iodo-2-buten-1-ol with organozincs and other organometals (Tetrahedron Letters, 1993)
- Synthesis of (R)-1-benzyloxy-3-buten-2-ol- a potential chiral synthon from L-(+)-tartaric acid: its applications in natural product syntheses (Tetrahedron Letters, 1987)
- Aspects of metabolism of tamoxifen by rat liver microsomes: Identification of a new metabolite: E-1-[4-(2-dimethylaminoethoxy)-phenyl]-1, 2-diphenyl-1-buten-3-ol N-oxide (Biochemical Pharmacology, 1986)
- Palladium-catalyzed conversion of esters of 4-(trimethylsilyl)-2-buten-1-ol to trimethylsilyl esters: a new carboxyl protecting group (Journal of Organic Chemistry, 1984)
- Unstable enols in the gas phase. Preparation ionization, energies, and heats of formation of (E)- and (Z)-2-buten-2-ol, 2-methyl-1-propen-1-ol, and 3-methyl-2-buten-2-ol (Journal of the American Chemical Society, 1988)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCC=CCO
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InChIKeyWCASXYBKJHWFMY-UHFFFAOYSA-N
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