1-Bromopentane

1-Bromopentane.svg 240px 2d structure of amyl bromide skin-invert 1-bromopentane vdw.png 240px bg-transparent 1-Bromopentane Amyl bromide n-Amyl bromide Pentyl bromide 110-53-2 1-BPPeBrn-PeBrnPeBrnPeBrAmBrn-AmBrnAmBrnAmBr 155850 47130 7766 203-776-0 8057 Z2S4R599P0 1993 InChI=1S/C5H11Br/c1-2-3-4-5-6/h2-5H2,1H3 YZWKKMVJZFACSU-UHFFFAOYSA-N CCCCCBr 5 11 1 Colorless liquid 1.22 g·cm−3 (20°C) 9.39mmHg (25 °C) 129.8 02 07 09 Warning H226 H315 H319 H335 H411 P210 P233 P240 P241 P242 P243 P261 P264 P264+P265 P271 P273 P280 P302+P352 P303+P361+P353 P304+P340 P305+P351+P338 P319 P321 P332+P317 P337+P317 P362+P364 P370+P378 P391 P403+P233 P403+P235 P405 P501 1-Bromopentane or amyl bromide is a bromoalkane and isomer of bromopentane. It is a colorless liquid. It is found as a natural product in Fucus vesiculosus.The LOTUS Initiative for Open Natural Products Research: frozen dataset union wikidata (with metadata) 2023 https://zenodo.org/records/7534071 en 10.5281/zenodo.7534071 Rutz Adriano Bisson Jonathan Allard Pierre-Marie 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. Dagani M. J. Barda H. J. Benya T. J. Sanders D. C. Bromine Compounds 10.1002/14356007.a04_405 It is also formed by the reaction of 1-pentanol with hydrogen bromide. See also Bromopentane References Category:Bromoalkanes