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Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

2-[4-[(2-methylpropan-2-yl)oxycarbonyl]piperazin-1-yl]-2-pyridin-3-ylacetic acid

O=C(N1CCN(CC1)C(c1cccnc1)C(=O)O)OC(C)(C)C Request for Quotation
Chemical Name: 2-[4-[(2-methylpropan-2-yl)oxycarbonyl]piperazin-1-yl]-2-pyridin-3-ylacetic acid
CAS Number: 885274-51-1
Product Number: AG0046CM(AGN-PC-0KKORI)
Synonyms:
MDL No:
Molecular Formula: C16H23N3O4
Molecular Weight: 321.3715

Identification/Properties

Properties
Storage:
Keep in dry area;2-8℃;

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


The compound 2-(4-(tert-Butoxycarbonyl)piperazin-1-yl)-2-(pyridin-3-yl)acetic acid, known as $name$, serves as a versatile building block in chemical synthesis, particularly in the field of medicinal chemistry and drug development. Its unique structure combines a piperazine moiety functionalized with a tert-butoxycarbonyl (Boc) protecting group and a pyridine ring attached to an acetic acid group.In organic synthesis, this compound can be used as a key intermediate for the preparation of various pharmaceuticals and bioactive molecules. The Boc protecting group on the piperazine nitrogen atom can be selectively removed under mild conditions, allowing for further derivatization or coupling reactions. The pyridine ring, on the other hand, provides a site for potential interactions with biological targets or metal catalysts.Moreover, the presence of both a basic piperazine functionality and an acidic carboxylic acid group in the molecule offers opportunities for molecular manipulation and modulation of physicochemical properties. By modifying the substituents on the piperazine and pyridine rings, chemists can fine-tune the compound's solubility, lipophilicity, and binding affinity to specific biological targets.Overall, the strategic placement of functional groups in $name$ enables chemists to access diverse chemical space and create novel compounds with potential therapeutic applications through rational design and synthesis strategies.