| Weight | 157.998 g/mol |
|---|---|
| Formula | C5H4BrN |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 0 |
3-BROMOPYRIDINE (626-55-1)
Score:
#45 in Inorganic chemistry
,
#2183 in Physics
,
#6753 in Chemistry
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- Effective lithiation of 3-bromopyridine: synthesis of 3-pyridine boronic acid and variously 3-substituted pyridines (Tetrahedron Letters, 2002)
- The Electrostatic Nature of ArylBromineHalide Synthons: The Role of ArylBromineHalide Synthons in the Crystal Structures of the trans-Bis(2-bromopyridine)dihalocopper(II) and trans-Bis(3-bromopyridine)dihalocopper(II) Complexes (Crystal Growth & Design, 2006)
- Spectral and X-ray structure determination of two polymeric complexes of copper(II) azide with 3-picoline and 2-bromopyridine: Cu(3-picoline)2(N3)2 and Cu(2-bromopyridine)(N3)2 (Polyhedron, 1992)
- Palladium-catalyzed reaction of 3-bromopyridine with allylic alcohols: a convenient synthesis of 3-alkylpyridines (Journal of Organic Chemistry, 1978)
- Regioselective arylation of 3-bromopyridine (Journal of Heterocyclic Chemistry, 1983)
- Ring opening metathesis polymerisation initiated by RuCl2(3-bromopyridine)2(H2IMes)(CHPh): Scope and limitation in block copolymer synthesis (Journal of Molecular Catalysis A-chemical, 2006)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=CC(=CN=C1)Br
-
InChIKeyNYPYPOZNGOXYSU-UHFFFAOYSA-N
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3-BROMOPYRIDINE
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