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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-Piperidinone, 1-(phenylmethyl)-, oxime

ON=C1CCN(CC1)Cc1ccccc1 Request for Quotation
Chemical Name: 4-Piperidinone, 1-(phenylmethyl)-, oxime
CAS Number: 949-69-9
Product Number: AG00678Q(AGN-PC-0JL9N7)
Synonyms:
MDL No:
Molecular Formula: C12H16N2O
Molecular Weight: 204.2682

Identification/Properties

Properties
BP:
338.5°C at 760 mmHg
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
204.273g/mol
XLogP3:
1.5
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
204.126g/mol
Monoisotopic Mass:
204.126g/mol
Topological Polar Surface Area:
35.8A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
212
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
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


1-Benzylpiperidin-4-one oxime is a versatile compound commonly used in chemical synthesis as a key intermediate in the production of various compounds. With its unique molecular structure, this compound serves as a valuable building block for the synthesis of a wide range of pharmaceuticals, agrochemicals, and specialty chemicals.In organic chemistry, 1-Benzylpiperidin-4-one oxime is frequently utilized in the creation of complex molecules through functional group transformations. Its reactivity allows for the introduction of various functional groups, facilitating the synthesis of diverse chemical entities with tailored properties.Moreover, this compound plays a crucial role in the development of new materials, such as polymers and catalysts, due to its ability to participate in a variety of chemical reactions. By serving as a starting material or an intermediate in synthetic pathways, 1-Benzylpiperidin-4-one oxime enables chemists to access sophisticated chemical structures efficiently.Overall, the application of 1-Benzylpiperidin-4-one oxime in chemical synthesis demonstrates its significance in the field of organic chemistry, offering researchers a powerful tool for the construction of complex molecules and the advancement of diverse areas of chemical science.