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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)-

2,5-Pyrrolidinedione, 3-methyl-3-phenyl-

O=C1NC(=O)CC1(C)c1ccccc1 Request for Quotation
Chemical Name: 2,5-Pyrrolidinedione, 3-methyl-3-phenyl-
CAS Number: 1497-17-2
Product Number: AG001LY2(AGN-PC-07Y4T9)
Synonyms:
MDL No:
Molecular Formula: C11H11NO2
Molecular Weight: 189.2105

Identification/Properties

Properties
MP:
83-85°C(lit.);
BP:
371.1°C at 760 mmHg
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
189.214g/mol
XLogP3:
1
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:
269
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#:
-
Hazard Statements:
H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-Methyl-2-phenylsuccinimide is a versatile compound widely used in chemical synthesis. One of its key applications is as a building block in the creation of various pharmaceuticals, agrochemicals, and other fine chemicals. Known for its unique chemical structure, 2-Methyl-2-phenylsuccinimide serves as a valuable intermediate in the synthesis of complex organic molecules. Through its involvement in diverse reactions such as amide formation, reduction, and substitution, this compound plays a crucial role in the development of a wide range of products with important industrial and commercial applications. Its ability to undergo various transformations under different reaction conditions makes it a valuable asset in the field of organic chemistry, enabling the synthesis of novel compounds with potential therapeutic, agricultural, or industrial benefits.