Chemistry Organic Building Blocks Aryls
Organic chemistry defines an aryl as a functional group or substituent derived from an aromatic ring, typically a hydrocarbon that is aromatic.
Aryl groups are commonly used as protecting groups. Certain types of phenyl derivatives can be cleaved by basic hydrolysis.
An aryl group is a functional group that is derived from an aromatic ring by removing one hydrogen atom. This functional group is often represented in chemical structures using the shorthand notation "Ar".
Arylation refers to the introduction of an aryl group into a molecule. This can be accomplished through various methods, including cross-coupling reactions, nucleophilic aromatic substitution, and electrophilic aromatic substitution.
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4-Amino-5-chloro-2-methoxy-N-(piperidin-4-ylmethyl)benzamide hydrochloride
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4-[(1,2,4-Triazole-1-yl)methyl]phenylhydrazine HCl
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1-(4-Fluorophenyl)-1h-pyrrole-2-carboxylic acid
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5-(4-Methoxyphenyl)-1,3,4-oxadiazol-2(3H)-one
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5-(4-(Trifluoromethyl)phenyl)-1,3,4-oxadiazol-2(3H)-one