cinnamic , auch: cinnamonic

Cinnamic alcohol was discovered only in the sample from Bulgaria.

Its supposed effectiveness against these ailments is attributed to the cinnamic acid found in the plants.

Another example is shown below, the photochemical dimerization of cinnamic acid.

Sinapyl alcohol is an organic compound derived from cinnamic acid.

Ethyl cinnamate is the ester of cinnamic acid and ethanol.

Work on alcohol, amber, benzoin resin and cinnamic acid.

Phenylpropanoic acid can be prepared from cinnamic acid by hydrogenation.

Cinnamic acid is also a kind of self-inhibitor produced by fungal spore to prevent germination.

These compounds are hydroxy derivatives of cinnamic acid.

Both mechanisms use cinnamic acid as their starting point, which is derived from the amino acid phenylalanine.

Allergic contact dermatitis and stomatitis caused by a cinnamic aldehyde-flavored toothpaste.

This efficiency is commonly associated with chemical structures incorporating several conjugated double bonds, as seen in the structure of cinnamic acid.

Cinnamic acid is a white crystalline organic acid, which is slightly soluble in water.

A laboratory synthesis of styrene entails the decarboxylation of cinnamic acid.

Company) have found that cinnamic aldehyde, when used in Big Red, prevented oral bacterial growth by more than 50%.

Cinnamaldehyde (cinnamic aldehyde) is a common fragrance allergen.

Milkweed oil from the seeds can be easily converted into cinnamic acid, which is a very potent sunscreen when used at a 1-5% concentration.

Phenylalanine is converted to cinnamic acid by the enzyme phenylalanine ammonia-lyase.

Cinnamic acid is also part of the biosynthetic shikimate and phenylpropanoid pathways.

The secret behind the polymer's ability is the addition of cinnamic acid or similar molecules, which can form or break bonds under light of certain wavelengths.

Examples of photoresponsive switches include cinnamic acid and cinnamylidene acetic acid.

His investigations in the aromatic series include isomerism of the cinnamic acids and the synthesis of tyrosine from phenylalanine (1882).

Recent research documents antimelanoma activity of cinnamic aldehyde observed in cell culture and a mouse model of human melanoma.

So have cinnamic acid, p-methoxycinnamic acid, and stigmasterol.

Only a few identified compounds, such as anigorufone and pinosylvin, use cinnamic acid as their start molecule.