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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)-

Piperazine, 2-(4-methoxyphenyl)-

COc1ccc(cc1)C1NCCNC1 Request for Quotation
Chemical Name: Piperazine, 2-(4-methoxyphenyl)-
CAS Number: 91517-26-9
Product Number: AG00GS13(AGN-PC-098ISC)
Synonyms:
MDL No:
Molecular Formula: C11H16N2O
Molecular Weight: 192.2575

Identification/Properties

Computed Properties
Molecular Weight:
192.262g/mol
XLogP3:
0.6
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
192.126g/mol
Monoisotopic Mass:
192.126g/mol
Topological Polar Surface Area:
33.3A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
167
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
1
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
Signal Word:
Danger
UN#:
3259
Hazard Statements:
H301-H315-H318
Precautionary Statements:
P280-P301+P310-P305+P351+P338
Class:
8
Packing Group:
Ⅲ

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-(4-Methoxyphenyl)piperazine, also known as 4-Methoxyphenylpiperazine or piperazine derivative, is a versatile compound widely utilized in chemical synthesis processes. This organic compound plays a significant role in pharmaceutical research and development due to its unique properties and diverse applications.One prominent application of 2-(4-Methoxyphenyl)piperazine is its use as a building block in the synthesis of various bioactive molecules and pharmaceutical compounds. Its structural flexibility and functional groups make it a valuable intermediate in the preparation of drug candidates, such as antipsychotics, antidepressants, and anti-inflammatory agents. By incorporating 2-(4-Methoxyphenyl)piperazine into molecular structures, chemists can modify the pharmacological properties and enhance the bioavailability of potential therapeutics.Additionally, 2-(4-Methoxyphenyl)piperazine is employed in the development of novel chemical entities for medicinal chemistry research. Its ability to interact with specific biological targets and exhibit pharmacological activity makes it a valuable scaffold for designing new drug leads. By exploring the reactivity of 2-(4-Methoxyphenyl)piperazine and its derivatives, researchers can create structurally diverse compounds with improved efficacy and reduced side effects.In summary, the application of 2-(4-Methoxyphenyl)piperazine in chemical synthesis provides a platform for innovation and discovery in the field of pharmaceuticals. Its versatility and potential for designing biologically active molecules make it an indispensable tool for medicinal chemists striving to develop safe and effective drugs for various therapeutic indications.