4-Hexynoic acid, 2-amino- is an organic compound characterized by the presence of both an alkyne and an amino group in its structure. It features a six-carbon chain with a triple bond between the fourth and fifth carbon atoms, along with an amino group (-NH2) attached to the second carbon. This compound is classified as an amino acid derivative and exhibits properties typical of both carboxylic acids and amines. It is likely to be a colorless to pale yellow liquid or solid, depending on its state at room temperature. The presence of the alkyne functional group contributes to its reactivity, allowing for potential participation in various chemical reactions, such as nucleophilic additions or coupling reactions. Additionally, the amino group can engage in hydrogen bonding, influencing its solubility in polar solvents. 4-Hexynoic acid, 2-amino- may have applications in organic synthesis, pharmaceuticals, or as a building block in the development of more complex molecules. However, specific safety and handling guidelines should be followed due to its chemical reactivity.

4-Hexynoic acid, 2-amino-

29834-75-1: 4-Hexynoic acid, 2-amino- is an organic compound characterized by the presence of both an alkyne and an amino group in its structure. It features a six-carbon chain with a triple bond between the fourth and fifth carbon atoms, along with an amino group (-NH2) attached to the second carbon. This compound is classified as an amino acid derivative and exhibits properties typical of both carboxylic acids and amines. It is likely to be a colorless to pale yellow liquid or solid, depending on its state at room temperature. The presence of the alkyne functional group contributes to its reactivity, allowing for potential participation in various chemical reactions, such as nucleophilic additions or coupling reactions. Additionally, the amino group can engage in hydrogen bonding, influencing its solubility in polar solvents. 4-Hexynoic acid, 2-amino- may have applications in organic synthesis, pharmaceuticals, or as a building block in the development of more complex molecules. However, specific safety and handling guidelines should be followed due to its chemical reactivity.

CAS 29834-75-1

4-Hexynoic acid, 2-amino-

2-Aminohex-4-ynoic acid

Ref: 3D-EBA83475