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CAS 71066-00-7

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N-BOC-2-Aminoindane-2-carboxylic acid

Description:
N-BOC-2-Aminoindane-2-carboxylic acid is a chemical compound characterized by its unique structure, which includes an indane ring system, an amino group, and a carboxylic acid functional group. The "N-BOC" designation refers to the tert-butyloxycarbonyl (BOC) protecting group attached to the amino nitrogen, which is commonly used in organic synthesis to protect amines during chemical reactions. This compound is typically utilized in the synthesis of various pharmaceuticals and bioactive molecules due to its ability to serve as a building block in peptide synthesis and other organic transformations. It is generally a white to off-white solid and is soluble in organic solvents, making it suitable for various laboratory applications. The presence of both the amino and carboxylic acid groups allows for potential interactions in biological systems, contributing to its relevance in medicinal chemistry. As with many chemical substances, proper handling and safety precautions should be observed, given its potential reactivity and the need for specific storage conditions.
Formula:C15H18NO4
InChI:InChI=1/C15H19NO4/c1-14(2,3)20-13(19)16-15(12(17)18)8-10-6-4-5-7-11(10)9-15/h4-7H,8-9H2,1-3H3,(H,16,19)(H,17,18)/p-1
SMILES:CC(C)(C)OC(=NC1(Cc2ccccc2C1)C(=O)[O-])O
Synonyms:
  • N-tert.-Butoxycarbonyl-2-aminoindane-2-carboxylic acid
  • BOC-2-Aic
  • 2-[(tert-butoxycarbonyl)amino]-2,3-dihydro-1H-indene-2-carboxylate
  • 2-(Boc-amino)indane-2-carboxylic Acid
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