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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)-

2H-Imidazol-2-one, 1,3-dihydro-4,5-dimethyl-

Cc1[nH]c(=O)[nH]c1C Request for Quotation
Chemical Name: 2H-Imidazol-2-one, 1,3-dihydro-4,5-dimethyl-
CAS Number: 1072-89-5
Product Number: AG007T7Q(AGN-PC-0LWTPU)
Synonyms:
MDL No:
Molecular Formula: C5H8N2O
Molecular Weight: 112.1298

Identification/Properties

Computed Properties
Molecular Weight:
112.132g/mol
XLogP3:
-0.1
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
0
Exact Mass:
112.064g/mol
Monoisotopic Mass:
112.064g/mol
Topological Polar Surface Area:
41.1A^2
Heavy Atom Count:
8
Formal Charge:
0
Complexity:
144
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#:
-
Hazard Statements:
H315-H319-H335
Precautionary Statements:
P233-P260-P261-P264-P270-P271-P280-P301+P312-P302+P352-P304-P304+P340-P305+P351+P338-P312-P321-P330-P332+P313-P337+P313-P340-P362-P403-P403+P233-P405-P501
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


4,5-Dimethyl-1H-imidazol-2(3H)-one is a versatile compound widely utilized in chemical synthesis as a key building block. With its unique structure, this compound serves as a crucial intermediate in the preparation of various pharmaceuticals, agrochemicals, and specialty chemicals. Its heterocyclic nature and functional groups enable it to participate in diverse reactions, such as alkylation, acylation, and cyclization, facilitating the formation of complex molecular structures. In particular, it is frequently employed in the synthesis of bioactive compounds, including antifungal agents, antibacterial drugs, and enzyme inhibitors. The strategic incorporation of 4,5-Dimethyl-1H-imidazol-2(3H)-one in synthetic pathways enables chemists to access a wide range of valuable molecules with enhanced biological activities and pharmacological properties.