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Cycloheptene is a 7-membered cycloalkene with a flash point of −6.7 °C. It is a raw material in organic chemistry and a monomer in polymer synthesis. Cycloheptene can exist as either the cis - or the trans -isomer.
Rhenium and molybdenum catalysts are used. Nowadays, only the reverse reaction, i.e., the conversion of ethylene and 2-butene to propylene is industrially practiced, however. [6] Shell higher olefin process (SHOP) produces (alpha-olefins) for conversion to detergents. The process recycles certain olefin fractions using metathesis. [7]
N,6-Dimethylhept-5-en-2-amine. CAS Number: 503-01-5 ... [2] Along with paracetamol and dichloralphenazone, it is one of the constituents of Amidrine. Chemistry
20 icosa- 900 nonacta- 21 henicosa- 1000 kilia- 22 docosa- 2000 dilia- 23 tricosa- 3000 trilia- 24 tetracosa- 4000 tetralia- 25 pentacosa- 5000 pentalia- 26
Heptene is a higher olefin, or alkene with the formula C 7 H 14. The commercial product is a liquid that is a mixture of isomers . It is used as an additive in lubricants, as a catalyst , and as a surfactant .
The synthesis of cyclohexanetetrols can be achieved by, among other methods: reduction or hydrogenation of (1) cyclohexenetetrols, (2) tri-hydroxycyclohexanones, (3) pentahydroxycyclohexanones, (4) hydroxylated aromatic hydrocarbons, or (5) hydroxylated quinones; the (6) hydrogenolysis of dibromocyclohexanetetrols; the (7) hydration of ...
Cyclohexene is a hydrocarbon with the formula (CH 2) 4 C 2 H 2. It is an example of a cycloalkene. At room temperature, cyclohexene is a colorless liquid with a sharp odor. Among its uses, it is an intermediate in the commercial synthesis of nylon. [3]
When cyclopentadiene is used as the diene, the vicinal norbornene diol bicyclo[2.2.1]hept-5-ene-2,3-diol is formed after hydrolysis. The Swern oxidation to the 1,2-ketone bicyclo[2.2.1]hept-5-ene-2,3-dione proceeds (in the variant with trifluoroacetic anhydride instead of oxalyl chloride ) with a yield of 73%.