| Weight | 241.935 g/mol |
|---|---|
| Formula | C4H2Br2S |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 0 |
2,3-Dibromothiophene (3140-93-0)
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- Lithiation reaction of 2,5-dibromothiophene. Carbon-13 NMR spectra of 3-substituted derivatives (Journal of Organic Chemistry, 1984)
- Synthesis of 2-Substituted 3,5-Dibromothiophenes through Base-catalyzed Halogen Dance Reaction of 2,5-Dibromothiophene (Heterocycles, 1983)
- Difference selective population inversion spectra and their application to the study of 13CH coupling constants in 2,3-dibromothiophene (Journal of Magnetic Resonance, 1974)
- Synthesis of functionalized benzothiophenes by twofold Heck and subsequent 6-electrocyclization reactions of 2,3-dibromothiophene (Tetrahedron Letters, 2009)
- Polymerization of 3-methyl-2,5-dibromothiophene utilizing n-butyl lithium and copper(II) chloride (Journal of Polymer Science: Polymer Letters Edition, 1984)
- 3,4 -Dibromothiophene from 2-Bromothiophene (Synthetic Communications, 1990)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=CSC(=C1Br)Br
-
InChIKeyATRJNSFQBYKFSM-UHFFFAOYSA-N
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