Weight | 185.846 g/mol |
---|---|
Formula | C2H2Br2 |
Hydrogen Acceptors | 0 |
Hydrogen Donors | 0 |
Aromatic Rings | 0 |
Rotatable Bonds | 0 |
1,2-DIBROMOETHYLENE (25429-23-6, 540-49-8)
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- Synthesis of stereoisomerically pube (E)-1,5-diyn-3-enes and (E)-1-bromo-3-yn-1-enes by diastereoselective palladium-catalyzed cross-coupling reaction of 1-alkynylzinc chlorides with a stereoisomeric mixture of 1,2-dibromoethylene. (Tetrahedron Letters, 1986)
- Palladium-mediated reactions between 1-alkynylzinc chlorides and (E)/(Z)-1,2-dibromoethylene or (E)-1,2-dibromo-1,2-diphenylethylene (Gazzetta Chimica Italiana, 1988)
- KINETICS, ISOTOPE RATE EFFECT, AND MECHANISM OF DEHYDROBROMINATION OF cis- 1,2-DIBROMOETHYLENE WITH TRIETHYLAMINE IN DIMETHYLFORMAMIDE. (Journal of the American Chemical Society, 1969)
- Dissociative adsorption and thermal desorption of dibromoethylene on Si(100)21: surface mediated dehalogenation and recombinative evolution of HBr (Surface Science, 2003)
- Photodissociation of 1,2Dibromoethylene at 248 nm: Br2 Molecular Elimination Probed by Cavity RingDown Absorption Spectroscopy (ChemPhysChem, 2008)
- Isotope enrichment and stereochemistry of the products from the reaction of electronically excited iodine monochloride with cis- and trans-1,2-dibromoethylene (Journal of the American Chemical Society, 1979)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC(=CBr)Br
-
InChIKeyUWTUEMKLYAGTNQ-UHFFFAOYSA-N
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Similar Compounds
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