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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)-

Benzenemethanamine, 4-(1-piperidinylmethyl)-

NCc1ccc(cc1)CN1CCCCC1 Request for Quotation
Chemical Name: Benzenemethanamine, 4-(1-piperidinylmethyl)-
CAS Number: 91271-81-7
Product Number: AG00GRZC(AGN-PC-0LOCGA)
Synonyms:
MDL No:
Molecular Formula: C13H20N2
Molecular Weight: 204.3113

Identification/Properties

Computed Properties
Molecular Weight:
204.317g/mol
XLogP3:
1.5
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

GHS Pictogram:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


4-(1-Piperidinylmethyl)benzenemethanamine, also known as $name$, is a versatile compound widely used in chemical synthesis processes. Its unique structure, combining a piperidine ring with a benzene moiety, confers several valuable properties that make it a valuable reagent in organic chemistry.In chemical synthesis, $name$ serves as a key building block for the preparation of various pharmaceuticals, agrochemicals, and other fine chemicals. Its piperidine group can undergo selective functionalization reactions, allowing for the introduction of different substituents at specific positions. This enables chemists to tailor the structure of the final products for desired properties and activities.Additionally, the benzene ring in $name$ provides aromaticity and stability to the molecule, making it an essential component in the synthesis of heterocyclic compounds and bioactive molecules. By incorporating 4-(1-Piperidinylmethyl)benzenemethanamine into synthetic pathways, chemists can access a diverse range of compounds with enhanced biological activities and improved pharmacokinetic profiles.Overall, the application of 4-(1-Piperidinylmethyl)benzenemethanamine in chemical synthesis offers a powerful tool for the preparation of complex organic molecules with tailored properties and functionalities. Its versatility and reactivity make it a valuable asset for researchers and synthetic chemists working in various fields of chemistry.