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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)-

Benzenamine, 4-[2-(1-piperidinyl)ethyl]-

Nc1ccc(cc1)CCN1CCCCC1 Request for Quotation
Chemical Name: Benzenamine, 4-[2-(1-piperidinyl)ethyl]-
CAS Number: 168897-21-0
Product Number: AG007V7J(AGN-PC-0N94I6)
Synonyms:
MDL No: MFCD04114506
Molecular Formula: C13H20N2
Molecular Weight: 204.3113

Identification/Properties

Computed Properties
Molecular Weight:
204.317g/mol
XLogP3:
2.4
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
3
Exact Mass:
204.163g/mol
Monoisotopic Mass:
204.163g/mol
Topological Polar Surface Area:
29.3A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
167
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


4-(2-(Piperidin-1-yl)ethyl)aniline is a versatile chemical compound widely used in organic synthesis. This compound plays a crucial role in the development and production of various pharmaceuticals, dyes, and other fine chemicals. In chemical synthesis, it serves as a key building block for the creation of complex molecules due to its unique structural properties. By incorporating 4-(2-(Piperidin-1-yl)ethyl)aniline into different synthetic pathways, chemists can effectively introduce specific functional groups and enhance the overall reactivity of the reaction. This compound's substituent groups and amine functionality make it an excellent candidate for introducing structural diversity and complexity into target molecules. Its application extends to the synthesis of biologically active compounds, heterocyclic systems, and specialty chemicals, making it a valuable tool in synthetic organic chemistry.