N-FMOC-4-amino-2-chlorobenzoic acid is a chemical compound characterized by its structure, which includes a 4-amino group and a 2-chloro substituent on a benzoic acid backbone, along with a fluorenylmethyloxycarbonyl (FMOC) protective group. This compound is typically used in peptide synthesis as a protecting group for amino acids, facilitating the selective modification of amino functionalities. The FMOC group is known for its stability under basic conditions and can be removed under mild acidic conditions, making it advantageous in synthetic chemistry. The presence of the chlorine atom introduces additional reactivity, allowing for further functionalization. N-FMOC-4-amino-2-chlorobenzoic acid is generally soluble in organic solvents, and its properties can be influenced by the pH of the solution due to the carboxylic acid group. This compound is utilized in various applications, including drug development and the synthesis of complex organic molecules, highlighting its importance in medicinal chemistry and biochemistry.

N-FMOC-4-AMINO-2-CHLOROBENZOIC ACID

186320-13-8: Fmoc-4-Amino-2-Chlorobenzoic Acid, Benzoic acid, 2-chloro-4-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]- (9CI)

4-(Fmoc-amino)-2-chloro-benzoic acid

4-Amino-2-chlorobenzoic acid, N-FMOC protected

CAS 186320-13-8: N-FMOC-4-AMINO-2-CHLOROBENZOIC ACID

N-FMOC-4-AMINO-2-CHLOROBENZOIC ACID

Ref: IN-DA00APCK

4-(Fmoc-amino)-2-chloro-benzoic acid

Ref: 3D-LHA32013

4-Amino-2-chlorobenzoic acid, N-FMOC protected

Ref: 54-OR307077

2-Chloro-4-{[(9h-fluoren-9-ylmethoxy)carbonyl]amino}benzoic acid

Ref: 10-F641060