3-(Boc-amino)benzoic acid, with the CAS number 111331-82-9, is a chemical compound characterized by the presence of a benzoic acid moiety substituted with a tert-butyloxycarbonyl (Boc) protected amino group at the meta position. The Boc group serves as a protective group for the amino functionality, making it stable under various conditions while allowing for deprotection when needed for further chemical reactions. This compound is typically a white to off-white solid and is soluble in organic solvents such as dichloromethane and dimethyl sulfoxide, but less soluble in water. It is often utilized in peptide synthesis and other organic synthesis applications due to its ability to facilitate the introduction of amino acids into larger molecular frameworks. The presence of both the carboxylic acid and the amino group allows for potential reactivity in coupling reactions, making it a valuable intermediate in medicinal chemistry and drug development. Proper handling and storage conditions should be observed, as with many organic compounds, to ensure stability and safety.

3-(boc-amino)benzoic acid

111331-82-9: Boc-3-Abz-OH, 3-(Tert-Butoxycarbonyl)-Amino Benzoic Acid, 3-[(Tert-Butoxycarbonyl)Amino]Benzoate

3-{[(tert-Butoxy)carbonyl]amino}benzoic acid

3-(Boc-Amino)benzoic acid

Boc-3-Abz-OH

3-(n-Boc amino)benzoic acid is a coupling agent that can be used in the synthesis of anilines. It has a chloride group and an aminobenzoic acid group. The compound is synthesized from terephthaloyl chloride and 3-aminobenzoic acid. This method is scalable, and 3-(n-Boc amino)benzoic acid is used to couple anilines with other chemical compounds.

CAS 111331-82-9: 3-(boc-amino)benzoic acid

3-{[(tert-Butoxy)carbonyl]amino}benzoic acid

Ref: 54-OR303920

3-(Boc-Amino)benzoic acid

Ref: 10-F236722

3-(Boc-Amino)benzoic acid

Ref: IN-DA003OFD

Boc-3-Abz-OH

Ref: 7W-GM7416

3-(n-Boc amino)benzoic acid

Ref: 3D-FB12600