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2-(3-((tert-butoxycarbonyl)amino)-2-oxo-2,3,4,5-tetrahydro-1H-benzo[b]azepin-1-yl)acetic acid
$360.00
CAS No.: 103105-97-1
Catalog No.: 192562
Purity: 95%
MF: C17H22N2O5
MW: 334.372
Storage: 2-8 degree Celsius
SMILES: C(C)(C)(C)OC(=O)NC1CCC2=C(N(C1=O)CC(=O)O)C=CC=C2
Catalog No.: 192562
Purity: 95%
MF: C17H22N2O5
MW: 334.372
Storage: 2-8 degree Celsius
SMILES: C(C)(C)(C)OC(=O)NC1CCC2=C(N(C1=O)CC(=O)O)C=CC=C2
2-(3-((tert-butoxycarbonyl)amino)-2-oxo-2,3,4,5-tetrahydro-1H-benzo[b]azepin-1-yl)acetic acid; CAS No.: 103105-97-1; 2-(3-((tert-butoxycarbonyl)amino)-2-oxo-2,3,4,5-tetrahydro-1H-benzo[b]azepin-1-yl)acetic acid. PROPERTIES: 2-(3-((Tert-butoxycarbonyl)amino)-2-oxo-2,3,4,5-tetrahydro-1H-benzo[b]azepin-1-yl)acetic acid exists as a white to pale yellow powder with a characteristic carboxylic acid odor. The compound demonstrates Boc protection behavior and shows moderate solubility in polar aprotic solvents. It exhibits zwitterionic character at physiological pH. Recommended storage involves maintaining in tightly sealed containers away from moisture. Safety protocols recommend avoiding dust inhalation and providing local exhaust ventilation as per ACGIH threshold limit values for organic acids. APPLICATIONS: 2-(3-((Tert-butoxycarbonyl)amino)-2-oxo-2,3,4,5-tetrahydro-1H-benzo[b]azepin-1-yl)acetic acid functions as an intermediate in the synthesis of calcineurin inhibitors documented in transplant immunology research. Its benzoazepine framework enables formation of bioactive peptidomimetics useful in protease inhibitor design as reported in medicinal chemistry communications. Furthermore, the compound contributes to synthesis of fluorescent probes for protein detection described in bioanalytical chemistry innovations.
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