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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)-

1-[(4-bromophenyl)methyl]piperidine

Brc1ccc(cc1)CN1CCCCC1 Request for Quotation
Chemical Name: 1-[(4-bromophenyl)methyl]piperidine
CAS Number: 178162-69-1
Product Number: AG0025TD(AGN-PC-010KVE)
Synonyms:
MDL No:
Molecular Formula: C12H16BrN
Molecular Weight: 254.1661

Identification/Properties

Computed Properties
Molecular Weight:
254.171g/mol
XLogP3:
3.3
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
2
Exact Mass:
253.047g/mol
Monoisotopic Mass:
253.047g/mol
Topological Polar Surface Area:
3.2A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
158
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#:
N/A
Hazard Statements:
H315-H319-H335-H401
Precautionary Statements:
P261-P273-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


1-(4-Bromobenzyl)piperidine is a versatile compound frequently utilized in chemical synthesis due to its unique reactivity and structural characteristics. In organic synthesis, this compound serves as a valuable building block for the preparation of various complex molecules in the pharmaceutical and agrochemical industries. The presence of the bromine atom on the benzyl ring imparts selective reactivity, allowing for strategic manipulation of the molecule during synthesis. Additionally, the piperidine moiety confers important pharmacological properties to the final products, making this compound a key intermediate in the production of bioactive compounds and drug candidates. The use of 1-(4-Bromobenzyl)piperidine in chemical synthesis enables chemists to access a wide range of target molecules with tailored properties for applications in medicinal chemistry and materials science.