2-Butenoic acid, 4-[[1,1-dimethylethoxy]carbonyl]amino]-, (2E)-, also known by its CAS number 180913-22-8, is an organic compound characterized by its structure, which includes a butenoic acid moiety with an amino group substituted at the fourth position. This compound features a dimethylethoxycarbonyl group, which enhances its stability and solubility in organic solvents. The (2E) designation indicates the configuration of the double bond in the butenoic acid portion, signifying that the higher priority substituents are on opposite sides of the double bond, which can influence its reactivity and interactions. Typically, compounds of this nature may exhibit properties such as moderate polarity, potential for hydrogen bonding due to the carboxylic acid and amino functionalities, and reactivity typical of both alkenes and carboxylic acids. These characteristics make it relevant in various chemical synthesis applications, particularly in the fields of pharmaceuticals and agrochemicals, where such derivatives can serve as intermediates or active ingredients.

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

180913-22-8: 2-Butenoic acid, 4-[[1,1-dimethylethoxy]carbonyl]amino]-, (2E)-, also known by its CAS number 180913-22-8, is an organic compound characterized by its structure, which includes a butenoic acid moiety with an amino group substituted at the fourth position. This compound features a dimethylethoxycarbonyl group, which enhances its stability and solubility in organic solvents. The (2E) designation indicates the configuration of the double bond in the butenoic acid portion, signifying that the higher priority substituents are on opposite sides of the double bond, which can influence its reactivity and interactions. Typically, compounds of this nature may exhibit properties such as moderate polarity, potential for hydrogen bonding due to the carboxylic acid and amino functionalities, and reactivity typical of both alkenes and carboxylic acids. These characteristics make it relevant in various chemical synthesis applications, particularly in the fields of pharmaceuticals and agrochemicals, where such derivatives can serve as intermediates or active ingredients.

CAS 180913-22-8

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

(2E)-4-([(tert-Butoxy)carbonyl]amino)but-2-enoic acid

Ref: IN-DA0022GR

(2E)-4-{[(tert-butoxy)carbonyl]amino}but-2-enoic acid

Ref: 10-F521131