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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, 3-(1-piperidinylmethyl)-

Nc1cccc(c1)CN1CCCCC1 Request for Quotation
Chemical Name: Benzenamine, 3-(1-piperidinylmethyl)-
CAS Number: 93138-55-7
Product Number: AG003HZO(AGN-PC-0LU5FP)
Synonyms:
MDL No: MFCD04114502
Molecular Formula: C12H18N2
Molecular Weight: 190.2847

Identification/Properties

Properties
MP:
106 °C
BP:
312.3°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
190.29g/mol
XLogP3:
2.5
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
2
Exact Mass:
190.147g/mol
Monoisotopic Mass:
190.147g/mol
Topological Polar Surface Area:
29.3A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
164
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

GHS Pictogram:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H319
Precautionary Statements:
P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


3-(Piperidin-1-ylmethyl)aniline, a versatile compound in chemical synthesis, serves as a crucial building block for the construction of various organic molecules. Its unique structure, containing both a piperidine ring and an aniline moiety, imparts significant reactivity, making it a valuable intermediate in the synthesis of pharmaceuticals, agrochemicals, and other fine chemicals. In organic synthesis, 3-(Piperidin-1-ylmethyl)aniline can be employed as a nucleophilic catalyst or as a precursor for the introduction of functional groups through various chemical reactions such as alkylation, acylation, and condensation reactions. This compound's presence in a molecule can serve to modulate its biological activity and enhance its pharmacological properties. Additionally, the structural features of 3-(Piperidin-1-ylmethyl)aniline allow for facile derivatization, enabling chemists to modify its structure to tailor the physical and chemical properties of the final product. This compound's utility in chemical synthesis extends its applications to the creation of diverse organic compounds with potential applications in medicinal chemistry and materials science.