| Weight | 124.998 g/mol |
|---|---|
| Formula | C4H6Cl2 |
| Hydrogen Acceptors | 0 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 1 |
1,3-Dichlorobut-2-ene
1,3-dichloro-2-butene
10075-38-4, 7415-31-8, 926-57-8
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- Reduction of 1,4-dichlorobut-2-yne by titanocene to a 1,2,3-butatriene. Formation of a 1-titanacyclopent-3-yne and a 2,5-dititanabicyclo[2.2.0]hex-1(4)-ene. (Chemical Communications, 2004)
- Arene-catalysed lithiation of 1,4-dichlorobut-2-enes and 3,4-dichlorobut-1-ene and reaction with electrophiles : a common reaction pathway (Tetrahedron, 1994)
- Improved synthesis of 3-cyclopentene-1-carboxylic acid from 1,4-dichloro-2-butene (Journal of Organic Chemistry, 1967)
- 1,3-Dipolar cycloaddition of a chiral nitrone to (E)-1,4-dichloro-2-butene: a new efficient synthesis of (2S,3S,4R)-4-hydroxyisoleucine (Tetrahedron Letters, 2012)
- Improved Preparation of Methyl 3-Chloro-2-Butenoate; Precursor of the Wichterle Annulation Reagent, 1,3-Dichloro-2-Butene (Synthetic Communications, 1981)
- 1,1-Dichloroethyl hydroperoxide and 1,1-dichloroethyl peroxide ion as intermediates in the ozonolysis of 2,3-dichloro-2-butene (Journal of Organic Chemistry, 1984)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - 1,3-dichloro-2-butene
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SMILESCC(=CCCl)Cl
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InChIKeyWLIADPFXSACYLS-UHFFFAOYSA-N
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1,3-Dichlorobut-2-ene
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