| Weight | 104.58 g/mol |
|---|---|
| Formula | C5H9Cl |
| Hydrogen Acceptors | 0 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 1 |
1-CHLORO-3-METHYL-2-BUTENE (503-60-6)
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- Allylic Rearrangement in the Reactions of 1-Chloro-3-methyl-2-butene; an Attempt at Total Synthesis of Geraniol (Journal of the American Chemical Society, 1954)
- Reactions of 1-Chloro-3-nitro-2-butene and Sodium 2-Propanenitronate; 3-Methyl-4-(2-nitro-2-propyl)-isoxazoline Oxide (Journal of the American Chemical Society, 1954)
- Improved Preparation of Methyl 3-Chloro-2-Butenoate; Precursor of the Wichterle Annulation Reagent, 1,3-Dichloro-2-Butene (Synthetic Communications, 1981)
- Preparation of 4,4,4-trifluoro-2-methyl-1-butene by the dehydrochlorination of 3-chloro-1,1,1-trifluoro-3-methylbutane, the preparation of 1,2-epoxy-4,4,4-trifluoro-2-methylbutane and the polymerization thereof (1990)
- One-pot synthesis of 3-chloro-1,1,2-trimethylindenes from trifluoromethanesulfonic acid catalyzed benzoylation of 2-methyl-2-butene (Journal of Organic Chemistry, 1988)
- Allylic Chlorides. VIII. 1-Chloro-3-methyl-2-butene (Journal of the American Chemical Society, 1949)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCC(=CCCl)C
-
InChIKeyJKXQKGNGJVZKFA-UHFFFAOYSA-N
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Synthesis
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1-Hydroxy-1,2-benziodoxol-3(1H)-one 1-oxide
(Nicolaou IBX dehydrogenation)
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1-CHLORO-3-METHYL-2-BUTENE
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