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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)-

tert-butyl 3-(4-hydroxyphenyl)piperazine-1-carboxylate

O=C(N1CCNC(C1)c1ccc(cc1)O)OC(C)(C)C Request for Quotation
Chemical Name: tert-butyl 3-(4-hydroxyphenyl)piperazine-1-carboxylate
CAS Number: 889956-81-4
Product Number: AG0046AK(AGN-PC-0156J1)
Synonyms:
MDL No:
Molecular Formula: C15H22N2O3
Molecular Weight: 278.3468

Identification/Properties

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

Safety Information

GHS Pictogram:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


1-Boc-3-(4-Hydroxyphenyl)piperazine is a versatile chemical compound widely utilized in chemical synthesis for a variety of applications. This compound serves as a key building block in the preparation of various pharmaceuticals, agrochemicals, and other biologically active molecules. Its unique structure and properties make it particularly valuable in the synthesis of complex organic compounds.In chemical synthesis, 1-Boc-3-(4-Hydroxyphenyl)piperazine can be used as a starting material for the construction of heterocyclic scaffolds, which are essential components in the design and development of novel drugs and molecular probes. By incorporating this compound into a synthesis pathway, chemists can introduce specific functionalities and stereochemical elements that are crucial for the desired biological activity of the final product.Furthermore, the presence of a Boc (tert-butoxycarbonyl) protecting group in 1-Boc-3-(4-Hydroxyphenyl)piperazine offers strategic advantages in organic synthesis. This protecting group can shield reactive functional groups during chemical transformations, enabling selective reactions at specific sites within the molecule. This level of control is crucial for achieving high yields and purities in multi-step syntheses.Overall, 1-Boc-3-(4-Hydroxyphenyl)piperazine plays a significant role in the field of chemical synthesis by providing chemists with a powerful tool for the efficient and precise construction of intricate molecular structures with potential applications in pharmaceutical and agrochemical research.