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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)-

Butanamide, N-methyl-3-oxo-

CNC(=O)CC(=O)C Request for Quotation
Chemical Name: Butanamide, N-methyl-3-oxo-
CAS Number: 20306-75-6
Product Number: AG0028O8(AGN-PC-0CJ1GG)
Synonyms:
MDL No:
Molecular Formula: C5H9NO2
Molecular Weight: 115.1305

Identification/Properties

Properties
MP:
-3 °C
BP:
279.4°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Form:
Liquid
Computed Properties
Molecular Weight:
115.132g/mol
XLogP3:
-0.6
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
2
Exact Mass:
115.063g/mol
Monoisotopic Mass:
115.063g/mol
Topological Polar Surface Area:
46.2A^2
Heavy Atom Count:
8
Formal Charge:
0
Complexity:
109
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-P271-P280-P302+P352-P304-P304+P340-P305+P351+P338-P312-P321-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


N-Methyl-3-oxobutanamide, also known as N-Methyl acetoacetamide, is a versatile chemical compound that finds wide applications in organic synthesis. This compound serves as a key building block in the preparation of various pharmaceuticals, agrochemicals, and fine chemicals due to its unique reactivity and functional groups.In chemical synthesis, N-Methyl-3-oxobutanamide acts as an important intermediate in the formation of complex molecules. Its beta-keto functionality allows for the facile introduction of diverse functional groups, enabling chemists to create a wide range of structurally diverse compounds. This compound can undergo various reactions such as condensations, reductions, and nucleophilic additions to generate a plethora of products with tailored properties.Furthermore, N-Methyl-3-oxobutanamide is commonly used in the synthesis of heterocyclic compounds, which are prevalent in pharmaceuticals and materials science. Its ability to participate in cyclization reactions makes it a valuable precursor for constructing diverse ring systems with potential biological activities.Overall, the versatility and reactivity of N-Methyl-3-oxobutanamide make it a valuable tool for organic chemists seeking to access complex molecular architectures efficiently and selectively. By utilizing this compound in chemical synthesis, researchers can explore new synthetic pathways and expedite the development of novel compounds with diverse applications.