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allyl caproate
allyl caproate

allyl stearate/va copolymer
allyl stearate/va copolymer

styrene/allyl benzoate copolymer
styrene/allyl benzoate copolymer

da:5-allyl-1,3-benzodioxol
da:5-allyl-1,3-benzodioxol

allyl butyrate; butanoato de 2-propenilo
allyl butyrate; 2-propenyl butanoate

steareth-10 allyl ether/acrylates copolymer
steareth-10 allyl ether/acrylates copolymer

allyl isovalerate; 3-metilbutanoato de 2-propenilo
allyl isovalerate; 2-propenyl 3-methylbutanoate

allyl alcohol has the structure h2c=ch-ch2oh.
===organic compounds===allyl alcohol, the parent of allylic alcohols, has the structure h2c=ch-ch2oh.

allyl cyclohexylacetate; ciclo-hexanoacetato de 2-propenilo
allyl cyclohexylacetate; 2-propenyl cyclohexane acetate

another example of a simple allyl compound is allyl chloride.
another example of a simple allyl compound is allyl chloride.

allyl cyclohexylpropionate; 3-ciclo-hexanopropanoato de 2-propenilo
allyl cyclohexylpropionate; 2-propenyl 3-cyclohexanepropanoate

benzylic groups are related to allyl groups; both show enhanced reactivity.
benzylic groups are related to allyl groups; both show enhanced reactivity.

==nomenclature and bonding==allyl is a widely used term in organic chemistry.
==nomenclature and bonding==allyl is a widely used term in organic chemistry.

a substância «allyl phenethyl ether» também pode conter álcool alílico como impureza.
the substance allyl phenethyl ether may contain allyl alcohol as impurity as well.

==allyl compounds==many substituents can be attached to the allyl group to give stable compounds.
==allyl derivatives==many substituents can be attached to the allyl group to give stable compounds.

===allyl ligands in organometallic chemistry===the allyl ligand is commonly encountered in organometallic chemistry.
===metal allyl complexes===the allyl ligand is commonly encountered in organometallic chemistry.

most commonly, allyl ligands bind to metals via all three carbon centers, the so-called η3-binding mode.
most commonly, allyl ligands bind to metals via all three carbon centers, the so-called η3-binding mode.

o comité científico da alimentação humana concluiu nos seus pareceres emitidos em 26 de setembro de 2001 que o 4-allyl-1,2-dimethoxybenzeno (methyleugenol) e o 1-allyl-4-methoxybenzeno (estragole) são genotóxicos.
the scientific committee on food concluded in its opinions expressed on 26 september 2001 that 4-allyl-1,2-dimethoxybenzene (methyleugenol) and 1-allyl-4-methoxybenzene (estragole) are genotoxic.