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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)-

2-Piperidinone, 3-bromo-1-(phenylmethyl)-

BrC1CCCN(C1=O)Cc1ccccc1 Request for Quotation
Chemical Name: 2-Piperidinone, 3-bromo-1-(phenylmethyl)-
CAS Number: 77868-86-1
Product Number: AG00GCR7(AGN-PC-0NK45I)
Synonyms:
MDL No:
Molecular Formula: C12H14BrNO
Molecular Weight: 268.1497

Identification/Properties

Computed Properties
Molecular Weight:
268.154g/mol
XLogP3:
2.5
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
2
Exact Mass:
267.026g/mol
Monoisotopic Mass:
267.026g/mol
Topological Polar Surface Area:
20.3A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
226
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
1
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


1-Benzyl-3-bromopiperidin-2-one, a versatile chemical compound, serves as a crucial building block in various organic synthesis processes. This compound plays a significant role in the preparation of diverse pharmaceuticals, agrochemicals, and materials due to its unique structural properties. In chemical synthesis, it acts as a key intermediate for the production of complex molecules by participating in key coupling reactions, ring transformations, and functional group modifications. Its distinct structure enables facile manipulation for the creation of a wide array of organic compounds with specific functional groups and stereochemistry. Additionally, 1-Benzyl-3-bromopiperidin-2-one's reactivity and compatibility with various reagents make it a valuable tool for chemists in designing and accessing novel molecules with potential applications in medicinal chemistry, materials science, and beyond. This compound's versatility and utility in chemical synthesis underscore its importance in advancing the synthesis of new and complex organic entities.