AA97317
Packsize | Purity | Availability | Price | Discounted Price | Quantity | |
---|---|---|---|---|---|---|
250mg | 97% | in stock | $15.00 | $10.00 | - + | |
5g | 97% | in stock | $17.00 | $12.00 | - + | |
10g | 97% | in stock | $22.00 | $16.00 | - + | |
25g | 97% | in stock | $54.00 | $38.00 | - + |
*All products are for research use only and not intended for human or animal use.
*All prices are in USD.
Catalog Number: | AA97317 |
Chemical Name: | 1,4-Di-boc-piperazine-2-carboxylic acid |
CAS Number: | 181955-79-3 |
Molecular Formula: | C15H26N2O6 |
Molecular Weight: | 330.3767 |
MDL Number: | MFCD02179115 |
SMILES: | O=C(N1CCN(C(C1)C(=O)O)C(=O)OC(C)(C)C)OC(C)(C)C |
Complexity: | 477 |
Covalently-Bonded Unit Count: | 1 |
Heavy Atom Count: | 23 |
Hydrogen Bond Acceptor Count: | 6 |
Hydrogen Bond Donor Count: | 1 |
Rotatable Bond Count: | 5 |
Undefined Atom Stereocenter Count: | 1 |
XLogP3: | 1.4 |
1,4-Di-Boc-piperazine-2-carboxylic acid is a valuable chemical reagent commonly used in organic synthesis. It serves as a versatile building block for the construction of various complex molecules and pharmaceutical intermediates. This compound is particularly useful for the protection of amine groups due to its Boc (tert-butyloxycarbonyl) protecting groups.In chemical synthesis, 1,4-Di-Boc-piperazine-2-carboxylic acid is frequently employed for the selective functionalization of amines, which allows chemists to control the reactivity of specific amine groups within a molecule. By utilizing this compound, researchers can carry out sequential reactions without affecting other functional groups present in the molecule.Moreover, the Boc protecting groups on 1,4-Di-Boc-piperazine-2-carboxylic acid can be conveniently removed under mild acidic conditions, leading to the deprotection of the amine functionality. This feature makes it a valuable tool in the synthesis of peptides, pharmaceuticals, and natural products where selective deprotection is crucial for the overall success of the synthetic pathway.Overall, 1,4-Di-Boc-piperazine-2-carboxylic acid plays a significant role in chemical synthesis by enabling the efficient and selective modification of amine groups, thereby facilitating the preparation of diverse organic compounds with high precision and control.