Ethyl 2-amino-6-chlorobenzoate, with the CAS number 172217-11-7, is an organic compound characterized by its aromatic structure and functional groups. It features a benzoate moiety with an ethyl ester group and an amino group positioned at the 2nd carbon, while a chlorine atom is substituted at the 6th position of the benzene ring. This compound is typically a white to off-white solid and is soluble in organic solvents, reflecting its hydrophobic characteristics due to the aromatic ring. Ethyl 2-amino-6-chlorobenzoate may exhibit biological activity, making it of interest in pharmaceutical research and development. Its chemical properties include potential reactivity due to the amino and chloro substituents, which can participate in various chemical reactions, such as nucleophilic substitutions or coupling reactions. The presence of the ethyl ester group also suggests potential applications in esterification and transesterification processes. Overall, this compound's unique structure and functional groups contribute to its potential utility in synthetic organic chemistry and medicinal applications.

ETHYL 2-AMINO-6-CHLOROBENZOATE

172217-11-7: Ethyl 2-amino-6-chlorobenzoate, with the CAS number 172217-11-7, is an organic compound characterized by its aromatic structure and functional groups. It features a benzoate moiety with an ethyl ester group and an amino group positioned at the 2nd carbon, while a chlorine atom is substituted at the 6th position of the benzene ring. This compound is typically a white to off-white solid and is soluble in organic solvents, reflecting its hydrophobic characteristics due to the aromatic ring. Ethyl 2-amino-6-chlorobenzoate may exhibit biological activity, making it of interest in pharmaceutical research and development. Its chemical properties include potential reactivity due to the amino and chloro substituents, which can participate in various chemical reactions, such as nucleophilic substitutions or coupling reactions. The presence of the ethyl ester group also suggests potential applications in esterification and transesterification processes. Overall, this compound's unique structure and functional groups contribute to its potential utility in synthetic organic chemistry and medicinal applications.

CAS 172217-11-7

ETHYL 2-AMINO-6-CHLOROBENZOATE

ETHYL 2-AMINO-6-CHLOROBENZOATE

Ref: IN-DA00AOK1

Ethyl 2-amino-6-chlorobenzoate

Ref: 54-OR956410

6-amino-2-chlorobenzoic acid ethyl ester, 98%

Ref: 10-F341700