logo
Home  > 2-((tert-Butoxycarbonyl)amino)cyclopropanecarboxylic acid

AV26552

1083181-22-9 | 2-((tert-Butoxycarbonyl)amino)cyclopropanecarboxylic acid

Packsize Purity Availability Price Discounted Price    Quantity
100mg 97% in stock $96.00 $68.00 -   +
250mg 97% in stock $146.00 $103.00 -   +
1g 97% in stock $398.00 $279.00 -   +
5g 97% in stock $1,772.00 $1,241.00 -   +

*All products are for research use only and not intended for human or animal use.

*All prices are in USD.

Description
Catalog Number: AV26552
Chemical Name: 2-((tert-Butoxycarbonyl)amino)cyclopropanecarboxylic acid
CAS Number: 1083181-22-9
Molecular Formula: C9H15NO4
Molecular Weight: 201.2197
MDL Number: MFCD11558998
SMILES: O=C(OC(C)(C)C)NC1CC1C(=O)O

 

Upstream Synthesis Route
  • 2-Boc-amino-cyclopropanecarboxylic acid is a versatile building block in chemical synthesis, commonly utilized as a key intermediate in the preparation of various pharmaceuticals and fine chemicals. Due to its unique cyclopropane ring structure and amino acid functionality, this compound can undergo a range of chemical transformations to introduce diverse functional groups into target molecules.One common application of 2-Boc-amino-cyclopropanecarboxylic acid is in the synthesis of peptide derivatives. By selectively deprotecting the Boc group and activating the carboxylic acid moiety, this compound can be coupled with other amino acids or peptide fragments to construct peptide chains with tailored sequences and properties. The cyclopropane ring present in the molecule can also serve as a rigid framework in peptide design, influencing the conformation and biological activity of the resulting peptides.Furthermore, 2-Boc-amino-cyclopropanecarboxylic acid can participate in various ring-closing and cross-coupling reactions to form complex heterocycles and biologically active compounds. Its ability to undergo stereo- and regioselective reactions makes it a valuable synthetic building block for creating molecular scaffolds with specific three-dimensional structures and properties.Overall, the versatility and reactivity of 2-Boc-amino-cyclopropanecarboxylic acid make it an indispensable tool in the toolbox of synthetic chemists for the efficient construction of diverse molecular architectures with applications in medicinal chemistry, materials science, and beyond.
FEATURED PRODUCTS