Ethyl 4-(tert-butoxycarbonylamino)benzoate, with the CAS number 110969-44-3, is an organic compound that belongs to the class of benzoate esters. It features a benzoic acid derivative where the carboxylic acid group is esterified with ethyl alcohol, and it contains a tert-butoxycarbonyl (Boc) protecting group on the amino functional group. This compound is typically characterized by its white to off-white crystalline solid form and is soluble in organic solvents such as dichloromethane and ethyl acetate, but has limited solubility in water. The presence of the Boc group makes it useful in organic synthesis, particularly in peptide chemistry, as it can protect amines during various reactions. Ethyl 4-(tert-butoxycarbonylamino)benzoate is often employed in the synthesis of pharmaceuticals and biologically active compounds, highlighting its significance in medicinal chemistry. Its stability under standard laboratory conditions and reactivity under specific conditions make it a valuable intermediate in synthetic pathways.

ETHYL 4-(TERT-BUTOXYCARBONYLAMINO)BENZOATE

110969-44-3: Ethyl 4-(tert-butoxycarbonylamino)benzoate, with the CAS number 110969-44-3, is an organic compound that belongs to the class of benzoate esters. It features a benzoic acid derivative where the carboxylic acid group is esterified with ethyl alcohol, and it contains a tert-butoxycarbonyl (Boc) protecting group on the amino functional group. This compound is typically characterized by its white to off-white crystalline solid form and is soluble in organic solvents such as dichloromethane and ethyl acetate, but has limited solubility in water. The presence of the Boc group makes it useful in organic synthesis, particularly in peptide chemistry, as it can protect amines during various reactions. Ethyl 4-(tert-butoxycarbonylamino)benzoate is often employed in the synthesis of pharmaceuticals and biologically active compounds, highlighting its significance in medicinal chemistry. Its stability under standard laboratory conditions and reactivity under specific conditions make it a valuable intermediate in synthetic pathways.

<p>Ethyl 4-[(tert-butoxycarbonyl)amino]benzoate</p>

CAS 110969-44-3

ETHYL 4-(TERT-BUTOXYCARBONYLAMINO)BENZOATE

Ethyl 4-[(tert-butoxycarbonyl)amino]benzoate

Ref: 54-OR72196

ETHYL 4-(TERT-BUTOXYCARBONYLAMINO)BENZOATE

Ref: 10-F474748