Examples of 'propenyl' in a sentence
Meaning of "propenyl"
Propenyl (noun) - A chemical compound containing a propenyl group, often used in organic chemistry or pharmaceutical research
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- A radical of propene (propylene).
How to use "propenyl" in a sentence
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propenyl
Unsaturated alkyl is preferably ethenyl propenyl or butenyl.
Propenyl ethers do not hydrosilate.
Examples of alkenyl include ethenyl and propenyl.
Examples are propenyl and cyclohexenyl.
Preferred alkenyl groups are ethenyl and propenyl.
Propenyl alcohol acts as a monofunctional initiator in a propylene oxide polymerization reaction.
An obvious option is to use a phenyl propenyl sulfone.
Propenyl compounds are isomeric with and less common than allyl compounds.
Examples of suitable radicals are ethenyl or propenyl.
The propenyl unsaturation removal step can be conducted batchwise or in a continuous manner.
The most preferred alkenyl carbonate is propenyl carbonate.
The propenyl double bond is available for crosslinking in the sulfur cure operation.
Examples of such groups include ethenyl and propenyl.
Propenyl stearate, polymer with ethenyl acetate.
Examples include ethenyl and propenyl.
See also
Vinyl, propenyl and isopropenyl groups are preferred.
Preferred alkenyl groups include ethenyl and propenyl.
Among these groups, a propenyl group is preferred.
Exemplary alkenyl groups include ethenyl and propenyl.
Alkenyl may be an allyl, propenyl or butenyl group.
Its chemical structure consists of a benzene ring substituted with a methoxy group and a propenyl group.
Examples include ethenyl, propenyl and butenyl.
Its chemical structure consists of a benzene ring substituted with a hydroxy group and a propenyl group.
Ethenyl, propenyl and butenyl are examples of alkenyl groups.
Examples of alkenyl groups include ethenyl and propenyl groups.
Propenyl ethers, such as the propenyl ether of propylene carbonate and compounds of formula.
The primary hydroxyl termination was produced as a result of cleavage of propenyl terminal groups.
Removal of the propenyl end-groups by refining gives polyols that have reduced unsaturation.
Exemplary alkenyl groups including one double bond include propenyl and butenyl.
Alkenyl is preferably ethenyl, propenyl or butenyl . Aryl is preferably phenyl or naphthyl.
That method was also the one used to determine initial propenyl ether content.
The propenyl ether content of the polyol of Example 5 is reduced as shown below.
The preferred alkenyl is ethenyl, propenyl or butenyl.
Propenyl polyether concentration, both entering and leaving the CSTR, and propionaldehyde generation are measured.
As alkenyl there is preferred ethenyl, propenyl or butenyl.
The propenyl group may occur as trans - and cis-isomers.
Example alkenyl groups include ethenyl, propenyl.
More particularly, it relates to a process to reduce propenyl polyethers in hydroxy-functional polyethers.
Preferably, alkenyl is ethenyl and propenyl.
A presently preferred alkenyl alkylating agent is propenyl quinoline t-butyl carbonate and a palladium catalyst.
The alkenyl of up to 4 carbon atoms are preferred such as allyl, propenyl or butenyl.
These polyols will generally not have propenyl end-group contents in excess of 30 mole percent.
Representative alkenyl groups include but are not limited to vinyl, allyl and propenyl.
Preferred alkenyl radicals are ethenyl, propenyl or butenyl radicals.
Examples of alkenyl include, but are not limited to, ethenyl and propenyl.
Alkenyl groups include ethenyl, propenyl and butenyl groups.
Additionally, Kramer discloses a fusión process for bringing together a bismaleimide compound and a propenyl compound.
Electron donor groups include vinyl ethers, propenyl ethers and other similar alkenyl ethers.
Compounds of formula I are useful starting products for the production of valuable 3-substituted propenyl cephalosporines.
Examples thereof include an allyl group, a propenyl group, a butenyl group, a cyclohexenyl group and the like.
