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1-Pentene is an alpha-olefin. Most often, 1-pentene is made as a byproduct of catalytic or thermal cracking of petroleum or during the production of ethylene and propylene via thermal cracking of hydrocarbon fractions. As of 2010s, the only commercial manufacturer of 1-pentene was Sasol Ltd., where it is separated from crude by the Fischer ...
1-Pentene (CAS 109-67-1) cis-2-Pentene (CAS 627-20-3) trans-2-pentene (CAS 646-04-8) Butenes. 2-Methyl-1-butene (CAS 563-46-2) 3-Methyl-1-butene (CAS 563-45-1)
English: 1-pentene structure, made using BKchem. Date: 1 February 2007 (original upload date) Source: Transferred from to Commons by Tomas_er using CommonsHelper.
Methylpentene is an alkene with a molecular formula C 6 H 12.The prefix "methyl-" is derived from the fact that there is a methyl(CH 3) branch, the word root "-pent-" is derived from the fact that there are 5 carbon atoms in the parent chain, while the "-ene" suffix denotes that there is a double bond present, as per IUPAC nomenclature. [1]
1-Pentyne is an organic compound with the formula CH 3 CH 2 CH 2 C≡CH. It is a terminal alkyne , in fact the smallest that is liquid at room temperature. The compound is a common terminal alkyne substrate in diverse studies of catalysis.
Polymethylpentene (PMP), also known as poly(4-methyl-1-pentene), is a thermoplastic polyolefin. It is used for gas-permeable packaging, autoclavable medical and laboratory equipment, microwave components, and cookware .
4-Methyl-1-pentene is used as a monomer for olefin polymerisation. The resulting polymer is poly(4-methyl-1-pentene). References This ...
1,4-Pentadiene can be prepared from 1,5-pentadiol via the diacetate. [6] 1,3-Pentadiene, like 1,3-butadiene, undergoes a variety of cycloaddition reactions. For example, it forms a sulfolene upon treatment with sulfur dioxide. [7]