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3-Bromopyridine
3-Bromopyridine is an aryl bromide and isomer of bromopyridine with the formula C5H4BrN. It is a colorless liquid that is mainly used as a building block in organic synthesis.
| Column 1 | Column 2 | Column 3 |
|---|---|---|
| Preferred IUPAC name | ||
| 3-Bromopyridine | ||
| CAS Number | .mw-parser-output .plainlist ol,.mw-parser-output .plainlist ul{line-height:inherit;list-style:none;margin:0;padding:0}.mw-parser-output .plainlist ol li,.mw-parser-output .plainlist ul li{margin-bottom:0}626-55-1 | |
| 3D model (JSmol) | Interactive image | |
| Beilstein Reference | 105880 | |
| ChEBI | CHEBI:51575 | |
| ChemSpider | 11783 | |
| ECHA InfoCard | 100.009.957 | |
| EC Number | 210-952-0 | |
| PubChem CID | 12286 | |
| UNII | XMN8H2XE9H | |
| CompTox Dashboard (EPA) | DTXSID9060819 | |
| InChI | ||
| InChI=1S/C5H4BrN/c6-5-2-1-3-7-4-5/h1-4HKey: NYPYPOZNGOXYSU-UHFFFAOYSA-N | ||
| SMILES | ||
| C1=CC(=CN=C1)Br | ||
| Chemical formula | C5H4BrN | |
| Molar mass | 157.998 g·mol−1 | |
| Appearance | colorless liquid | |
| Density | 1.640 g/cm3 | |
| Melting point | −27 °C (−17 °F; 246 K) | |
| Boiling point | 173 °C (343 °F; 446 K) | |
| GHS labelling: | ||
| Pictograms | ||
| Signal word | Danger | |
| Hazard statements | H226, H301, H302, H311, H315, H319, H332, H335 | |
| Precautionary statements | P210, P233, P240, P241, P242, P243, P261, P264, P270, P271, P280, P301+P310, P301+P312, P302+P352, P303+P361+P353, P304+P312, P304+P340, P305+P351+P338, P312, P321, P322, P330, P332+P313, P337+P313, P361, P362, P363, P370+P378, P403+P233, P403+P235, P405, P501 | |
| Flash point | 51 °C (124 °F; 324 K) | |
| Related compounds | 3-Chloropyridine2-Bromopyridine | |
| Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). |
Infobox references | | |
3-Bromopyridine is an aryl bromide and isomer of bromopyridine with the formula C5H4BrN. It is a colorless liquid that is mainly used as a building block in organic synthesis.
It participates as a substrate in many reactions associated with aryl halides, e.g., the Heck reaction and Buchwald–Hartwig amination.
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