Chemistry:1-Bromopentane: Difference between revisions
From HandWiki
| imported>S.Timg  simplify | imported>S.Timg  simplify | 
| (No difference) | |
Latest revision as of 02:03, 6 February 2024
| Error creating thumbnail: Unable to save thumbnail to destination | |
| Error creating thumbnail: Unable to save thumbnail to destination | |
| Names | |
|---|---|
| IUPAC name 1-Bromopentane | |
| Other names 
 | |
| Identifiers | |
| 3D model (JSmol) | |
| ChEMBL | |
| ChemSpider | |
| EC Number | 
 | 
| PubChem CID | |
| UNII | |
| UN number | 1993 | 
| 
 | |
| 
 | |
| Properties | |
| C5H11Br | |
| Molar mass | 151.047 g·mol−1 | 
| Appearance | Colorless liquid | 
| Density | 1.22 g·cm−3 (20 °C) | 
| Boiling point | 129.8 °C (265.6 °F; 402.9 K) | 
| Vapor pressure | 9.39 mmHg (25 °C) | 
| Hazards | |
| GHS pictograms |     | 
| GHS Signal word | Warning | 
| Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
| Infobox references | |
Tracking categories (test):
1-Bromopentane or amyl bromide is an isomer of bromopentane. It is a colorless liquid. It is found as a natural product in Fucus vesiculosus.[1]
Preparation
Most 1-bromoalkanes are prepared by free-radical addition of hydrogen bromide to the 1-alkene, which is 1-pentene in the case of 1-bromopentane. These conditions lead to anti-Markovnikov addition, giving the 1-bromo derivative.[2]
It is also formed by the reaction of 1-pentanol with hydrogen bromide.
See also
References
- ↑ Rutz, Adriano; Bisson, Jonathan; Allard, Pierre-Marie (2023). "The LOTUS Initiative for Open Natural Products Research: frozen dataset union wikidata (with metadata)" (in en). doi:10.5281/zenodo.7534071. https://zenodo.org/records/7534071.
- ↑ Dagani, M. J.; Barda, H. J.; Benya, T. J.; Sanders, D. C.. "Ullmann's Encyclopedia of Industrial Chemistry". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a04_405.
|  | 


