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3-Methylcyclohexene an organic compound consisting of cyclohexene with a methyl group substituent adjacent to the alkene group. Two other structural isomers are known: 1-methylcyclohexene and 4-methylcyclohexene. All are colorless volatile liquids classified as a cyclic olefins. They are specialized reagents.
1-Methylcyclohexene an organic compound consisting of cyclohexene with a methyl group substituent attached to the alkene group. Two other structural isomers are known: 3-methylcyclohexene and 4-methylcyclohexene. All are colorless volatile liquids. They are specialized reagents. Methylcyclohexenes are a cyclic olefins.
4-Methylcyclohexene is an organic compound consisting of cyclohexene with a methyl group substituent attached to carbon most distant from the alkene group. Two other structural isomers are known: 1-methylcyclohexene and 3-methylcyclohexene. All are colorless volatile liquids classified as a cyclic olefins. They are specialized reagents.
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]
5-Methyl-3-heptanone: 524 mg/m 3: 100 ppm: 541855: 60-34-4: 0180: Methyl hydrazine: 37.8 mg/m 3: 20 ppm: 60344, carcinogenic substance 74-88-4: 0509: Methyl iodide: 580 mg/m 3: 100 ppm: 74884, carcinogenic substance 108-11-2: 0665: Methyl isobutyl carbinol: 1672 mg/m 3: 400 ppm: 108112: 624-83-9: 0004: Methyl isocyanate: 7 mg/m 3: 3 ppm: 624839 ...
Allylic strain in an olefin. Allylic strain (also known as A 1,3 strain, 1,3-allylic strain, or A-strain) in organic chemistry is a type of strain energy resulting from the interaction between a substituent on one end of an olefin (a synonym for an alkene) with an allylic substituent on the other end. [1]
For example, CH 3-CH 3 is the alkane ethANe. The name of CH 2 =CH 2 is therefore ethENe . For straight-chain alkenes with 4 or more carbon atoms, that name does not completely identify the compound.
Cyclohexanol is produced by the oxidation of cyclohexane in air, typically using cobalt catalysts: [5]. 2 C 6 H 12 + O 2 → 2 C 6 H 11 OH. This process coforms cyclohexanone, and this mixture ("KA oil" for ketone-alcohol oil) is the main feedstock for the production of adipic acid.