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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, 3,3,4,4-tetramethyl-

O=C1NC(=O)C(C1(C)C)(C)C Request for Quotation
Chemical Name: 2,5-Pyrrolidinedione, 3,3,4,4-tetramethyl-
CAS Number: 3566-61-8
Product Number: AG0039EN(AGN-PC-0JLATO)
Synonyms:
MDL No:
Molecular Formula: C8H13NO2
Molecular Weight: 155.1943

Identification/Properties

Computed Properties
Molecular Weight:
155.197g/mol
XLogP3:
0.8
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
155.095g/mol
Monoisotopic Mass:
155.095g/mol
Topological Polar Surface Area:
46.2A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
204
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:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


3,3,4,4-Tetramethylpyrrolidine-2,5-Dione, commonly known as $name$, is a versatile compound widely utilized in chemical synthesis due to its unique properties and reactivity. In organic chemistry, $name$ serves as an important building block in the preparation of various pharmaceuticals, agrochemicals, and specialty chemicals.One of the key applications of 3,3,4,4-Tetramethylpyrrolidine-2,5-Dione in chemical synthesis is its use as a chiral auxiliary. By attaching $name$ to a substrate, chemists can control the stereochemistry of a reaction and selectively produce enantiomerically pure compounds. This is particularly valuable in the synthesis of complex molecules where precise stereochemical control is essential for the desired biological activity or physical properties.Furthermore, 3,3,4,4-Tetramethylpyrrolidine-2,5-Dione can also act as a catalyst or reagent in various organic transformations. Its unique structure allows it to participate in a range of reactions such as asymmetric Diels-Alder reactions, Michael additions, and aldol reactions, enabling the efficient and selective formation of new carbon-carbon and carbon-heteroatom bonds.Overall, the versatile nature of 3,3,4,4-Tetramethylpyrrolidine-2,5-Dione makes it a valuable tool in the hands of synthetic chemists for the development of novel chemical compounds with diverse applications in the fields of pharmaceuticals, materials science, and agrochemicals.