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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)-

Acetamide, N-(1-methyl-2-oxopropyl)-

CC(=O)NC(C(=O)C)C Request for Quotation
Chemical Name: Acetamide, N-(1-methyl-2-oxopropyl)-
CAS Number: 6628-81-5
Product Number: AG006O21(AGN-PC-0JM2RS)
Synonyms:
MDL No:
Molecular Formula: C6H11NO2
Molecular Weight: 129.1570

Identification/Properties

Properties
Storage:
Keep in dry area;2-8℃;
Computed Properties
Molecular Weight:
129.159g/mol
XLogP3:
-0.3
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
2
Exact Mass:
129.079g/mol
Monoisotopic Mass:
129.079g/mol
Topological Polar Surface Area:
46.2A^2
Heavy Atom Count:
9
Formal Charge:
0
Complexity:
131
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


N-(3-Oxobutan-2-yl)acetamide, also known as $name$, is a versatile compound widely used in chemical synthesis for its unique properties and reactivity. In organic chemistry, $name$ serves as a key building block for the synthesis of various complex molecules due to its ability to undergo different chemical reactions.One of the primary applications of N-(3-Oxobutan-2-yl)acetamide is its role as a precursor in the formation of heterocyclic compounds. This compound can participate in cyclization reactions, leading to the formation of cyclic structures with diverse functionalities. Additionally, $name$ can be utilized as a starting material for the synthesis of pharmaceutical intermediates, agrochemicals, and specialty chemicals.Moreover, N-(3-Oxobutan-2-yl)acetamide exhibits interesting reactivity in asymmetric synthesis. Its chiral nature allows for the creation of enantiomerically pure compounds, making it a valuable tool in the preparation of optically active molecules. By leveraging the reactivity of $name$, chemists can access a wide range of stereochemically complex compounds with high levels of enantiomeric purity.Overall, N-(3-Oxobutan-2-yl)acetamide plays a crucial role in the field of chemical synthesis, offering synthetic chemists a versatile building block to access a diverse array of structurally complex and biologically relevant compounds.