Examples of 'cinnamyl' in a sentence
Meaning of "cinnamyl"
cinnamyl (noun) - Referring to a chemical compound derived from cinnamic acid, commonly used in perfumery and flavoring
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- The univalent radical C₆H₅-CH=CH-CH₂- characteristic of cinnamic compounds
How to use "cinnamyl" in a sentence
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cinnamyl
The standard formula of the cinnamyl radical is.
They are known as a cinnamyl alcohol glycoside belonging to a group of compounds known as phenylpropanoids.
The preservative effect of cinnamyl alcohol.
These cinnamyl compounds give the cloudberry seed oil its typical odor.
Clinical data on the use of cinnamyl acetate in pregnancy are absent.
An example for aralkenyl is cinnamyl.
Epoxidation of cinnamyl alcohol can conveniently be carried out on a commercially scale using peracetic acid.
Suitable specific examples of the arylalkenyl groups include cinnamyl.
The doll sample was found to contain cinnamyl alcohol and coumarin.
Cinnamyl alcohol and related compounds are also present in cinnamon oil and cinnamon bark.
Specific examples of such groups are the styryl and cinnamyl groups.
Cinnamyl alcohol was discovered only in the sample from Bulgaria.
Rosarin and rosavin are cinnamyl alcohol glycosides isolated from Rhodiola rosea.
Cinnamyl acetate, used in fragrances and as flavour ingredient, has been discussed by several institutions.
How to detect Cinnamyl alcohol.
See also
For example, cinnamyl alcohol can readily be oxidized to cinnamaldehyde in a number of biological situations.
These compounds are cinnamaldehyde, cinnamyl alcohol, and closely related compounds.
The flavor composition also includes at least one non-aldehyde cinnamyl compound.
Rosarin is a cinnamyl alcohol glycoside isolated from Rhodiola rosea.
Esters of cinnamic acid such as amyl cinnamate, cinnamyl cinnamate and methyl cinnamate ;.
Rosavin is a cinnamyl alcohol glycoside found in the plant Rhodiola rosea.
Carbonate hydroxy protecting groups include methyl vinyl, allyl, cinnamyl and benzyl.
In other embodiments, the non-aldehyde cinnamyl compound is at least partially encapsulated.
EXAMPLE 5 This Example illustrates the preparation of cinnamyl aldehyde.
Under no conditions was cinnamyl alcohol produced using Pd / C.
Cinnamyl 2-methylcrotonate mixture of isomers.
Example 6 Transdermal drug delivery systems with cinnamyl alcohol as the active substance.
The final compounds 91-93 were synthesised using these experimental conditions and starting from cinnamyl chloride.
Alternatively, epoxidation of cinnamyl alcohols using known methods e . g.
Examples include ethyl acetate, amyl butyrate, and cinnamyl formate.
The concentration of cinnamyl alcohol was determined according to example 8 to 0.14 mg per cm ².
Example 8 This example illustrates the conversion of cinnamyl alcohol to the corresponding acid.
A compound according to claim 30 wherein G represents cinnamyl.
Mention may also be made of substituted or unsubstituted cinnamyl alcohols corresponding to formula [ 10 ].
Preparation of the various cinnamyl ester derivatives 3-6 utilizes cinnamic acid derivative, compound 33, as a key intermediate.
The target enzyme for controlling lignin production is cinnamyl alcohol dehydrogenase ( CAD ).
The cinnamyl acids may include, for example, cinnamic acid, 3-phenylpmpionic acid and combinations thereof.
When the thermolysis of 1a was run with added TEMPO, methoxycarbonyl and cinnamyl radicals were captured.
Key words, cinnamyl acetates, photochemistry, E / Z isomerization, photocleavage, fluorescence.
In another preferred embodiment R4 is optionally substituted cinnamyl ; preferably unsubstituted cinnamyl.
Example 7, General procedure for preparation of 3-Aryl-propylenediamines from cinnamyl aldehydes,.
The method of Example 14 is repeated, replacing cinnamyl methacrylate by vinylnorbornyl acrylate.
By “ aryl ” is meant a phenyl, naphthyl or cinnamyl group.
Figure 23 shows the molecular structure of surface bound cinnamyl bromide ; R represents the surface plus cross-linker.
The " ar ( lower ) alkenyl " represented by R4 includes phenylalkenyls such as cinnamyl and styryl.
The degree of conversion of ethyl cinnamyl carbonate was 60 %.
Cinnamaldehyde can be prepared synthetically, for example, by oxidation of cinnamyl alcohol Traynelis et al ., J.
Alcohols such as anise alcohol, geraniol, cinnamyl alcohol, menthol and linalool ;.
The ar ( lower ) alkenyl " for R4 includes phenylalkenyls such as cinnamyl and styryl.
Other esters include t-butyl, cyclopentyl, cyclohexyl, allyl, cinnamyl and phenyl, inclusing m-methylthiophenyl.
