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A copper chromite catalyst is usually used industrially. [1] The cis/trans ratio of the CHDM is affected by the catalyst. [2] Byproduct of this process are 4-methylcyclohexanemethanol (CH 3 C 6 H 10 CH 2 OH) and the monoester methyl 4-methyl-4-cyclohexanecarboxylate (CH 3 C 6 H 10 CO 2 CH 3, CAS registry number 51181-40-9). [3]
Systematically, it is called a but-2-en-1-yl group and exhibits geometric isomerism, being either cis (Z) or trans (E). There are many simple compounds in which the crotyl group forms base carbon chain: crotyl alcohol , crotonaldehyde , crotonic acid , and crotyl acrylate are examples.
1,4-Cyclohexadiene is an organic compound with the formula C 6 H 8. It is a colourless, flammable liquid that is of academic interest as a prototype of a large class of related compounds called terpenoids, an example being γ-terpinene. An isomer of this compound is 1,3-cyclohexadiene.
[4] [5] [6] These reactions are metal-catalyzed and proceed through a metallacyclobutane intermediate. [7] It was first published by Dider Villemin in 1980 describing the synthesis of an Exaltolide precursor, [ 8 ] and later become popularized by Robert H. Grubbs and Richard R. Schrock , who shared the Nobel Prize in Chemistry , along with Yves ...
[1] The general chemical formula of the halogen addition reaction is: C=C + X 2 → X−C−C−X (X represents the halogens bromine or chlorine, and in this case, a solvent could be CH 2 Cl 2 or CCl 4). The product is a vicinal dihalide. This type of reaction is a halogenation and an electrophilic addition.
1,4-Cyclohexanedimethanol diglycidyl ether is an organic chemical in the glycidyl ether family. [2] Its formula is C 14 H 24 O 4 and the IUPAC name is 2-[[4-(oxiran-2-ylmethoxymethyl)cyclohexyl]methoxymethyl]oxirane. It has the CAS number of 14228-73-0 [3] and is REACH registered in Europe. [4]
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.
It is a cyclohexane ring functionalized with an alcohol, specifically a hydroxymethyl group. The compound is a colorless liquid, although commercial samples can appear yellow. The compound is a colorless liquid, although commercial samples can appear yellow.