| Weight | 236.894 g/mol |
|---|---|
| Formula | C5H3Br2N |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 0 |
2,4-dibromopyridine (58530-53-3)
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- Density functional theory calculations and vibrational spectra of 3,5-dibromopyridine and 3,5-dichloro-2,4,6-trifluoropyridine (Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy, 2005)
- Regioselectivity in alkenyl(aryl)-heteroaryl Suzuki cross-coupling reactions of 2,4-dibromopyridine. A synthetic and mechanistic study (Tetrahedron, 2006)
- Ring transformations in reactions of heterocyclic halogeno compounds with nucleophiles (iii) conversion of 2,6-dibromopyridine by potassium amide in liquid ammonia into 4-amino-2-methylpyrimidine (Recueil des Travaux Chimiques des Pays-Bas, 2010)
- Synthesis of 2,4-dibromopyridine and 4,4'-dibromo-2,2'-bipyridine. Efficient usage in selective bromine-substitution under palladium-catalysis (Heterocycles, 2008)
- On the formation of 2,3,4,6tetrabromopyridine during the bromination of 2,6dibromopyridine at about 500: (43th Communication on derivatives of pyridine and quinoline.) (Recueil des Travaux Chimiques des Pays-Bas, 1939)
- Chemoselective Staudinger-Phosphite Reaction on the Azido Groups of 2,4,6-Triazido-3,5-dibromopyridine (Journal of Heterocyclic Chemistry, 2016)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=CN=C(C=C1Br)Br
-
InChIKeyPCMMSLVJMKQWMQ-UHFFFAOYSA-N
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