2-(5-amino-1H-pyrazol-3-yl)-pyrrolidine-1-carboxylic acid tert-butyl ester
$300.00
CAS No.: 1396967-66-0
Catalog No.: WLZ1864
Purity: 95%
MF: C12H20N4O2
MW: 252.318
Storage: 2-8 degree Celsius
SMILES: C(C)(C)(C)OC(=O)N1C(CCC1)C1=NNC(=C1)N
Catalog No.: WLZ1864
Purity: 95%
MF: C12H20N4O2
MW: 252.318
Storage: 2-8 degree Celsius
SMILES: C(C)(C)(C)OC(=O)N1C(CCC1)C1=NNC(=C1)N
CAS NO.: 1396967-66-0; 2-(5-amino-1H-pyrazol-3-yl)-pyrrolidine-1-carboxylic acid tert-butyl ester. PROPERTIES: This protected amino acid features a tert-butoxycarbonyl (Boc) group attached to a pyrrolidine ring connected to a pyrazolyl group, creating a molecule with potential applications in peptide synthesis and organic chemistry. The 2-(5-amino-1H-pyrazol-3-yl)-pyrrolidine-1-carboxylic acid tert-butyl ester typically appears as a white to off-white crystalline solid with moderate solubility in common organic solvents. Its molecular structure includes a Boc protecting group that can be selectively removed under acidic conditions. For optimal stability and to prevent premature deprotection, this compound should be stored at 2-8 degree Celsius in a tightly sealed container under anhydrous conditions. When handling, appropriate safety measures including nitrile gloves and safety goggles are essential. This compound is sensitive to moisture and may hydrolyze in aqueous environments. In case of accidental spillage, clean the area with a damp cloth and dispose of materials according to local regulations. APPLICATIONS: The 2-(5-amino-1H-pyrazol-3-yl)-pyrrolidine-1-carboxylic acid tert-butyl ester serves as a versatile building block in organic synthesis, particularly for creating pyrazolyl-substituted amines. The Boc protecting group provides a handle for further functionalization through selective deprotection. In peptide synthesis, this compound functions as a building block for developing peptide mimetics and other bioactive molecules. The pyrazolyl group contributes to target binding affinity and selectivity. Additionally, the molecule finds utility in materials science as a monomer for creating polymers with specific electronic and optical properties. Researchers utilizing this compound benefit from its functional group versatility, enabling the development of diverse molecular architectures for applications ranging from drug discovery to advanced materials.
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