| Weight | 399.727 g/mol |
|---|---|
| Formula | C4Br4S |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 0 |
Tetrabromothiophene (3958-03-0)
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- Measurement and correlation of the solubility of 2,3,4,5-tetrabromothiophene in different solvents (The Journal of Chemical Thermodynamics, 2012)
- Regioselective Palladium(0)-Catalyzed Cross-Coupling Reactions and Metal-Halide Exchange Reactions of Tetrabromothiophene: Optimization, Scope and Limitations (Advanced Synthesis & Catalysis, 2009)
- Synthesis of tetraarylthiophenes by regioselective Suzuki cross-coupling reactions of tetrabromothiophene (Tetrahedron Letters, 2007)
- Selective mono- to perarylations of tetrabromothiophene by a cyclobutene-1,2-diylbisimidazolium preligand. (Journal of Organic Chemistry, 2011)
- Tetrabromothiophene from 2-Bromothiophene by means of Sodium Acetylide in Liquid Ammonia (Nature, 1951)
- Synthesis of dibenzothiophenes and carbazoles by sequential 'tetra-fold heck/6 -electrocyclization/dehydrogenation' reactions of tetrabromothiophene and tetrabromo-N-methylpyrrole (Advanced Synthesis & Catalysis, 2012)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1(=C(SC(=C1Br)Br)Br)Br
-
InChIKeyAVPWUAFYDNQGNZ-UHFFFAOYSA-N
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Tetrabromothiophene
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