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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 4-(4-formyl-3-hydroxyphenyl)piperazine-1-carboxylate

O=Cc1ccc(cc1O)N1CCN(CC1)C(=O)OC(C)(C)C Request for Quotation
Chemical Name: tert-butyl 4-(4-formyl-3-hydroxyphenyl)piperazine-1-carboxylate
CAS Number: 1446332-69-9
Product Number: AG001JW3(AGN-PC-0JK2CY)
Synonyms:
MDL No:
Molecular Formula: C16H22N2O4
Molecular Weight: 306.3569

Identification/Properties

Computed Properties
Molecular Weight:
306.362g/mol
XLogP3:
2.4
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
4
Exact Mass:
306.158g/mol
Monoisotopic Mass:
306.158g/mol
Topological Polar Surface Area:
70.1A^2
Heavy Atom Count:
22
Formal Charge:
0
Complexity:
399
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


The tert-Butyl 4-(4-formyl-3-hydroxyphenyl)piperazine-1-carboxylate is a versatile compound widely used in chemical synthesis, particularly in the pharmaceutical and agrochemical industries. It serves as a key building block in the production of various organic compounds due to its unique structure and reactivity.This compound is commonly employed as a reagent in the synthesis of complex molecules, including pharmaceutical intermediates and potential drug candidates. Its functional groups, such as the formyl and hydroxyphenyl moieties, allow for selective chemical reactions to occur, enabling the creation of specific molecular structures with desired properties.In chemical synthesis, tert-Butyl 4-(4-formyl-3-hydroxyphenyl)piperazine-1-carboxylate can participate in a range of transformations, such as condensation reactions, nucleophilic additions, and cross-coupling reactions. These reactions enable the incorporation of the compound into target molecules or the modification of its structure to generate novel derivatives with enhanced biological activities.Overall, the application of tert-Butyl 4-(4-formyl-3-hydroxyphenyl)piperazine-1-carboxylate in chemical synthesis offers a valuable tool for researchers and chemists in the development of new compounds with potential therapeutic or agricultural applications.