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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]methyl]benzoic acid

O=C(N1CCN(CC1)Cc1ccccc1C(=O)O)OC(C)(C)C Request for Quotation
Chemical Name: 2-[[4-[(2-methylpropan-2-yl)oxycarbonyl]piperazin-1-yl]methyl]benzoic acid
CAS Number: 914349-53-4
Product Number: AG006AQO(AGN-PC-079RWH)
Synonyms:
MDL No:
Molecular Formula: C17H24N2O4
Molecular Weight: 320.3835

Identification/Properties

Properties
BP:
445.8 °C at 760 mmHg
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)methyl)benzoic acid plays a crucial role in chemical synthesis as a versatile building block for the preparation of various pharmaceuticals, agrochemicals, and materials. Its unique structure combines a piperazine ring functionalized with a tert-butoxycarbonyl protecting group attached to a benzoic acid moiety, offering multiple reactivity sites for selective chemical transformations.In chemical synthesis, this compound serves as a key intermediate for the creation of diverse bioactive molecules through strategic synthetic manipulations. The piperazine unit provides a nitrogen-containing heterocycle that can participate in important medicinal chemistry interactions, such as binding to biological targets or enhancing pharmacokinetic properties. The tert-butoxycarbonyl protecting group shields the piperazine amine functionality, allowing for selective modification of other reactive sites without unwanted side reactions.By utilizing 2-((4-(tert-Butoxycarbonyl)piperazin-1-yl)methyl)benzoic acid as a starting material or intermediate in chemical synthesis, researchers can access a wide range of structurally complex compounds with tailored properties for pharmaceutical development or material science applications. Its versatility and reactivity make it a valuable compound in the pursuit of novel molecules with potential therapeutic or industrial significance.