2-Butynoic acid, 4-[[1,1-dimethylethoxy]carbonyl]amino] (CAS 168762-94-5) is an organic compound characterized by its unique structure, which includes a butynoic acid moiety and a carbamate functional group. This compound features a triple bond between the second and third carbon atoms of the butynoic acid chain, contributing to its reactivity and potential applications in organic synthesis. The presence of the 1,1-dimethylethoxycarbonyl group enhances its stability and solubility in organic solvents. As an amino acid derivative, it may exhibit properties relevant to biological systems, such as potential interactions with enzymes or receptors. The compound is likely to be a solid at room temperature, with a specific melting point and boiling point that depend on its molecular weight and intermolecular forces. Its synthesis and characterization are of interest in medicinal chemistry and materials science, where it may serve as a building block for more complex molecules or as a precursor in various chemical reactions. Safety data should be consulted for handling and storage, as with all chemical substances.

2-Butynoicacid,4-[[(1,1-dimethylethoxy)carbonyl]amino]-(9CI)

168762-94-5: 2-Butynoic acid, 4-[[1,1-dimethylethoxy]carbonyl]amino] (CAS 168762-94-5) is an organic compound characterized by its unique structure, which includes a butynoic acid moiety and a carbamate functional group. This compound features a triple bond between the second and third carbon atoms of the butynoic acid chain, contributing to its reactivity and potential applications in organic synthesis. The presence of the 1,1-dimethylethoxycarbonyl group enhances its stability and solubility in organic solvents. As an amino acid derivative, it may exhibit properties relevant to biological systems, such as potential interactions with enzymes or receptors. The compound is likely to be a solid at room temperature, with a specific melting point and boiling point that depend on its molecular weight and intermolecular forces. Its synthesis and characterization are of interest in medicinal chemistry and materials science, where it may serve as a building block for more complex molecules or as a precursor in various chemical reactions. Safety data should be consulted for handling and storage, as with all chemical substances.

CAS 168762-94-5

2-Butynoicacid,4-[[(1,1-dimethylethoxy)carbonyl]amino]-(9CI)

2-Butynoic acid, 4-[[(1,1-dimethylethoxy)carbonyl]amino]-

Ref: IN-DA001Y9C

4-[(tert-Butoxycarbonyl)amino]but-2-ynoic acid

Ref: 54-OR43679

4-(TERT-BUTOXYCARBONYLAMINO)BUT-2-YNOIC ACID

Ref: 10-F471843

4-(tert-Butoxycarbonylamino)but-2-ynoic Acid

Ref: 3D-TGA76294