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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)-

[4-[(4-ethylpiperazin-1-yl)methyl]phenyl]methanamine

CCN1CCN(CC1)Cc1ccc(cc1)CN Request for Quotation
Chemical Name: [4-[(4-ethylpiperazin-1-yl)methyl]phenyl]methanamine
CAS Number: 914349-67-0
Product Number: AG00GV1T(AGN-PC-015QJ6)
Synonyms:
MDL No:
Molecular Formula: C14H23N3
Molecular Weight: 233.3525

Identification/Properties

Computed Properties
Molecular Weight:
233.359g/mol
XLogP3:
0.8
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
4
Exact Mass:
233.189g/mol
Monoisotopic Mass:
233.189g/mol
Topological Polar Surface Area:
32.5A^2
Heavy Atom Count:
17
Formal Charge:
0
Complexity:
204
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-(4-Ethylpiperazin-1-ylmethyl)benzylamine is a versatile compound widely utilized in chemical synthesis for its unique properties. When incorporated into reactions, this compound serves as an essential building block for the creation of various organic molecules, pharmaceuticals, and materials. Its functionality as a benzylamine derivative enables it to participate in key synthetic processes, offering chemists a valuable tool for designing and constructing complex chemical structures. Additionally, the presence of the piperazine ring in its structure imparts specific reactivity and functionality that can be exploited in the synthesis of diverse compounds. Overall, 4-(4-Ethylpiperazin-1-ylmethyl)benzylamine is a valuable asset in the realm of chemical synthesis, facilitating the development of new substances with varied applications.