Examples of 'is cyclohexyl' in a sentence
Meaning of "is cyclohexyl"
is cyclohexyl - Cyclohexyl is a term used in chemistry to describe a chemical compound or group that contains a cyclohexane ring structure. It's commonly found in organic compounds and can have various properties and applications
How to use "is cyclohexyl" in a sentence
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is cyclohexyl
The most preferred carbocyclic group is cyclohexyl.
Is cyclohexyl or an optionally substituted phenyl or pyridylring.
A preferred example of a cycloalkyl itaconate is cyclohexyl itaconate.
Preferred as R1 is cyclohexyl or cyclopropylmethyl, more preferably cyclohexyl.
The most preferred cycloalkyl is cyclohexyl.
Most preferably, R1 is cyclohexyl substituted by hydroxy.
The preferred cycloalkyl group is cyclohexyl.
In some embodiments, R2 is cyclohexyl optionally substituted.
An especially preferred ring is cyclohexyl.
For example, when R is cyclohexyl the four possible avermectins are,.
A preferred cycloalkyl group is cyclohexyl.
In some embodiments, R1 is cyclohexyl which is optionally substituted with from 1 to 3 independently selected R6.
Another suitable external donor is cyclohexyl trimethoxy silane.
Preferred are cyclopropyl and cyclohexyl ; and most preferred is cyclohexyl.
Preferred cycloalkylisocyanate is cyclohexyl isocyanate carbomoyl.
See also
Preferred monocyclic cycloalkyl rings include cyclopentyl, fluorocyclopentyl and cyclohexyl ; more preferred is cyclohexyl.
A particular example of cycloalkyl is cyclohexyl or cyclopropyl.
In one preferred embodiment R3 is cyclopentyl, in another preferred embodiment R3 is cyclohexyl.
Preferred one is cyclohexyl.
A compound, salt or solvate according to any previous claim wherein R is cyclohexyl.
The composition of claim 1 wherein R is cyclohexyl or tertiarybutyl cyclohexyl.
The preferred side-chain protecting group for Asp is cyclohexyl.
The vulcanization activator ( g ) is cyclohexyl benzothiazylsulphonamide.
The ungelled reaction product of claim 5 wherein R is cyclohexyl.
A compound as claimed in claim 1, wherein R1 is cyclohexyl or optionally substitued substituted C1-C6 alkyl.
A particular example of cycloalkyl is cyclohexyl.
In another embodiment, R3 is cyclohexyl substituted with R3a.
In a further embodiment, cycloalkyl is cyclohexyl.
Particularly " carbocyclyl " is cyclohexyl or phenyl.
Another aspect of the invention is a compound of formula I where R3 is cyclohexyl.
The process of claim 8 wherein R is cyclohexyl and R1 is ethyl.
Other preferred acids include those wherein R1 is hydroxyl and R2 is cyclohexyl.
A specific example is cyclohexyl.
A compound as claimed in any one of claims 1 to 4 in which R3 is cyclohexyl.
A preferred example is cyclohexyl.
A compound according to claim 1, characterized in that R6 is cyclohexyl.
In yet another embodiment the preferred substituent R5 is cyclohexyl or 4 - tert - butylphenyl.
A compound as claimed in claim 1 or claim 2 in which R3 is cyclohexyl.
The compound described in claim 4, wherein R1 is cyclohexyl or cyclopropylmethyl.
In another embodiment of the present invention, R2 is cyclohexyl.
A metal complex of Claim 13 where R * is cyclohexyl or isopropyl.
In still another embodiment, cycloalkyl residue R2 is cyclohexyl.
Particularly preferred is cyclohexyl.
Most preferably, ring A, together with X and the atoms to which X is bound, is cyclohexyl.
New compounds according to claim 1, wherein R2 is cyclohexyl or cyclopentyl.
A compound as claimed in any one of claims 1 to4 wherein R2 is cyclohexyl.
More preferably, the cyclic alkyl is cyclohexyl.
A compound of formula I according to claims 1 to 4, wherein D is cyclohexyl.
Most preferably, cycloalkyl is cyclohexyl.
In a particular embodiment of this invention, R8 is cyclohexyl.
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Examples of using Cyclohexyl
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Cyclopentyl and cyclohexyl are preferred cycloalkyl groups
Cycloalkyl groups are preferably cyclopentyl and cyclohexyl
Cyclohexyl group is preferable among these groups
