Amino(4-isopropylphenyl)acetic acid, also known by its CAS number 126746-20-1, is an organic compound characterized by the presence of an amino group, a phenyl ring substituted with an isopropyl group, and an acetic acid moiety. This compound typically exhibits properties associated with amino acids, including the ability to participate in hydrogen bonding due to its amino and carboxylic acid functional groups. The isopropyl substitution on the phenyl ring contributes to its hydrophobic characteristics, potentially influencing its solubility and interaction with biological systems. The compound may exhibit biological activity, making it of interest in pharmaceutical research, particularly in the development of drugs targeting specific receptors or pathways. Its structural features suggest that it could engage in various chemical reactions, including esterification and amide formation, which are common in organic synthesis. Overall, amino(4-isopropylphenyl)acetic acid represents a versatile building block in organic chemistry and medicinal chemistry applications.

AMINO(4-ISOPROPYLPHENYL)ACETIC ACID

126746-20-1: Amino(4-isopropylphenyl)acetic acid, also known by its CAS number 126746-20-1, is an organic compound characterized by the presence of an amino group, a phenyl ring substituted with an isopropyl group, and an acetic acid moiety. This compound typically exhibits properties associated with amino acids, including the ability to participate in hydrogen bonding due to its amino and carboxylic acid functional groups. The isopropyl substitution on the phenyl ring contributes to its hydrophobic characteristics, potentially influencing its solubility and interaction with biological systems. The compound may exhibit biological activity, making it of interest in pharmaceutical research, particularly in the development of drugs targeting specific receptors or pathways. Its structural features suggest that it could engage in various chemical reactions, including esterification and amide formation, which are common in organic synthesis. Overall, amino(4-isopropylphenyl)acetic acid represents a versatile building block in organic chemistry and medicinal chemistry applications.

Benzeneacetic acid, α-amino-4-(1-methylethyl)-

<p>2-Amino-2-(4-isopropylphenyl)acetic acid</p>

CAS 126746-20-1

AMINO(4-ISOPROPYLPHENYL)ACETIC ACID

Benzeneacetic acid, α-amino-4-(1-methylethyl)-

Ref: IN-DA000T6G

2-Amino-2-(4-isopropylphenyl)acetic acid

Ref: 54-OR480450

2-Amino-2-(4-isopropylphenyl)acetic acid

Ref: 10-F682197