Chemistry:1-Bromopentane
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Names | |
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IUPAC name
1-Bromopentane
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Other names
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Identifiers | |
3D model (JSmol)
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ChEMBL | |
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PubChem CID
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UNII | |
UN number | 1993 |
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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). | |
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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.
Original source: https://en.wikipedia.org/wiki/1-Bromopentane.
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