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Home  > 1,4-Di-boc-piperazine-2-carboxylic acid

AA97317

181955-79-3 | 1,4-Di-boc-piperazine-2-carboxylic acid

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.

Description
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

 

Computed Properties
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  

 

 

Upstream Synthesis Route
  • 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.
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