3-Aminophenylacetic acid, N-BOC protected, is a chemical compound characterized by the presence of an amino group and a carboxylic acid group attached to a phenyl ring, with a tert-butyloxycarbonyl (BOC) protecting group on the amino functionality. This compound is typically used in organic synthesis, particularly in the preparation of peptides and other nitrogen-containing compounds, as the BOC group provides a means to protect the amine during various chemical reactions. The BOC group is stable under basic conditions but can be removed under acidic conditions, allowing for selective deprotection when needed. The presence of both the amino and carboxylic acid groups makes this compound amphoteric, capable of acting as both an acid and a base. Its solubility characteristics are influenced by the functional groups present, often making it soluble in polar solvents. Overall, 3-Aminophenylacetic acid, N-BOC protected, serves as a valuable intermediate in pharmaceutical and chemical research, facilitating the synthesis of more complex molecules.

3-Aminophenylacetic acid, N-BOC protected

123036-51-1: N-Boc-3-Aminophenylacetic Acid, {3-[(Tert-Butoxycarbonyl)Amino]Phenyl}Acetic Acid

3-tert-Butoxycarbonylaminophenyl acetic acid

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CAS 123036-51-1: 3-Aminophenylacetic acid, N-BOC protected

3-tert-Butoxycarbonylaminophenyl acetic acid

Ref: 10-F023488

Boc-3-aminophenylacetic acid

Ref: 3D-FB49897

Benzeneacetic acid, 3-[[(1,1-dimethylethoxy)carbonyl]amino]-

Ref: IN-DA000JZW

3-[(tert-Butoxycarbonyl)amino]phenylacetic acid

Ref: 54-OR0181