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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, 1-(9H-fluoren-9-yl)-

N1CCN(CC1)C1c2ccccc2c2c1cccc2 Request for Quotation
Chemical Name: Piperazine, 1-(9H-fluoren-9-yl)-
CAS Number: 129604-54-2
Product Number: AG009GQJ(AGN-PC-0JQTR6)
Synonyms:
MDL No:
Molecular Formula: C17H18N2
Molecular Weight: 250.3382

Identification/Properties

Computed Properties
Molecular Weight:
250.345g/mol
XLogP3:
2.5
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
250.147g/mol
Monoisotopic Mass:
250.147g/mol
Topological Polar Surface Area:
15.3A^2
Heavy Atom Count:
19
Formal Charge:
0
Complexity:
288
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


1-(9H-fluoren-9-yl)piperazine hydrochloride is a versatile compound widely utilized in chemical synthesis as a key intermediate in the production of various pharmaceuticals, agrochemicals, and specialty chemicals. This compound acts as a valuable building block due to its unique chemical structure, which allows for the introduction of diverse functional groups and enables the synthesis of complex molecules. In organic synthesis, 1-(9H-fluoren-9-yl)piperazine hydrochloride serves as a crucial reagent in the formation of heterocyclic compounds, such as polycyclic aromatic compounds and nitrogen-containing rings. Additionally, it can be employed in the preparation of novel materials with tailored properties, including fluorescent dyes, liquid crystals, and coordination complexes. Its compatibility with a wide range of reaction conditions and its ability to undergo various transformations make it a valuable tool for chemists seeking to access structurally diverse and biologically active compounds.