Examples of 'cycloalkyl' in a sentence
Meaning of "cycloalkyl"
cycloalkyl (noun): Cycloalkyl refers to a type of organic compound where the carbon atoms form a closed ring structure with all carbon-carbon bonds being single bonds
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- Any univalent radical derived from a cycloalkane by removal of an atom of hydrogen
How to use "cycloalkyl" in a sentence
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cycloalkyl
Cycloalkyl groups are examples of saturated carbocyclic radicals.
More particular monocyclic cycloalkyl group is cyclopropyl.
Cycloalkyl represents a saturated cyclic aliphatic group.
An example of aryl fused with cycloalkyl is tetrahydronaphthalenyl.
Cycloalkyl includes the cis or trans forms.
The rings in a cycloalkyl group are not aromatic.
Cycloalkyl groups are preferably cyclopentyl and cyclohexyl.
Particularly preferred cycloalkyl groups are cyclopentyl or cyclohexyl.
Cycloalkyl includes monocyclic or bicyclic hydrocarbyl groups.
A particularly preferred cycloalkyl group is an adamantyl group.
The cycloalkyl group can be linear or branched.
Ligands generally correspond to alkyl or cycloalkyl chains.
Exemplary fused cycloalkyl groups include decahydronaphthalene.
Is a hydrogen atom or an alkyl or cycloalkyl radical and.
Each alkyl or cycloalkyl can be saturated or unsaturated.
See also
A specific example of a carbocyclyl group is a cycloalkyl group.
Exemplary cycloalkyl groups are cyclohexyl and norbomyl.
Preferred are the corresponding unsubstituted cycloalkyl groups.
Particular cycloalkyl groups are cyclopropyl and cyclohexyl.
The cyclopropyl group is a preferred cycloalkyl moiety.
Examples of cycloalkyl and cycloalkenyl are described above.
A is preferably lower alkyl and lower cycloalkyl.
More preferred cycloalkyl groups include cyclopropyl.
The alkyl groups include also cycloalkyl.
Preferred cycloalkyl rings are cyclopropyl and cyclopentyl.
Certain representative carbocycles are cycloalkyl as described above e.
Particular cycloalkyl are unsubstituted or substituted with alkyl.
The ring substituent a excludes cycloalkyl as defined in subgroup b.
Preferred cycloalkyl groups are cyclopentyl and cyclohexyl.
Preferably an alkylene or cycloalkyl is not substituted.
Cycloalkyl groups or moieties are preferably cyclopentyl or cyclohexyl.
A preferred example of a cycloalkyl itaconate is cyclohexyl itaconate.
Cycloalkyl groups are saturated unless otherwise defined.
Examples of polycyclic cycloalkyl groups are adamantane and norbornane.
Cycloalkyl groups may also be substituted by alkyl.
Examples of polycyclic cycloalkyl groups are adamantan and norbornane.
Cycloalkyl groups are monocyclic or bicyclic ring systems.
The most preferred cycloalkyl is cyclohexyl.
The cycloalkyl can be optionally substituted or unsubstituted.
Examples of an unsaturated cycloalkyl include cyclohexenyl.
The cycloalkyl group is preferably a cyclopropyl group.
A particular example of cycloalkyl is cyclohexyl or cyclopropyl.
The cycloalkyl moiety may be substituted or unsubstituted.
Examples include cycloalkyl and cycloalkenyl.
Cycloalkyl can optionally be substituted as defined herein.
Examples of polycyclic cycloalkyl radicals are adamantane and norbornane.
Cycloalkyl group is a cyclic alkyl group.
The preferred cycloalkyl group is cyclopentyl.
Cycloalkyl groups include hydroxycyclopentyl or methoxycyclohexyl.
The preferred cycloalkyl group is cyclohexyl.
