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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)-

2,4-Piperidinedione, 6-phenyl-

O=C1CC(=O)NC(C1)c1ccccc1 Request for Quotation
Chemical Name: 2,4-Piperidinedione, 6-phenyl-
CAS Number: 118264-04-3
Product Number: AG000ILQ(AGN-PC-00F3PN)
Synonyms:
MDL No: MFCD10568157
Molecular Formula: C11H11NO2
Molecular Weight: 189.2105

Identification/Properties

Properties
BP:
440.1°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Computed Properties
Molecular Weight:
189.214g/mol
XLogP3:
0.7
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
189.079g/mol
Monoisotopic Mass:
189.079g/mol
Topological Polar Surface Area:
46.2A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
244
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:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-H315-H319
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


6-Phenylpiperidine-2,4-dione, also known as PPD, is a versatile chemical compound widely utilized in chemical synthesis processes. This compound plays a crucial role as a building block in the synthesis of various pharmaceuticals, agrochemicals, and other organic compounds. Due to its unique structure and reactivity, 6-Phenylpiperidine-2,4-dione serves as a key intermediate in the production of diverse chemical substances.In chemical synthesis, 6-Phenylpiperidine-2,4-dione acts as a valuable precursor for the creation of complex molecules with specific pharmacological or biological properties. Its piperidine ring provides a stable scaffold for further functionalization through various chemical reactions, allowing researchers to introduce specific functional groups and modifications to tailor the final product for a particular application.Moreover, 6-Phenylpiperidine-2,4-dione exhibits excellent compatibility with a wide range of reagents and reaction conditions, making it a versatile tool for organic chemists and medicinal chemists alike. Its structural features offer opportunities for stereochemical control and regioselectivity in synthetic pathways, enabling the construction of structurally diverse compounds efficiently.Overall, the strategic incorporation of 6-Phenylpiperidine-2,4-dione in chemical synthesis enables the efficient and controlled assembly of complex molecular architectures, making it an indispensable component in the development of novel compounds with desired properties and functionalities.