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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)-

Ethanone, 1-(4,6-dimethyl-2-pyridinyl)-

Cc1cc(C)nc(c1)C(=O)C Request for Quotation
Chemical Name: Ethanone, 1-(4,6-dimethyl-2-pyridinyl)-
CAS Number: 59576-31-7
Product Number: AG00EIG3(AGN-PC-03X7D8)
Synonyms:
MDL No:
Molecular Formula: C9H11NO
Molecular Weight: 149.1897

Identification/Properties

Properties
BP:
241.2°C at 760 mmHg
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
149.193g/mol
XLogP3:
1.6
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
149.084g/mol
Monoisotopic Mass:
149.084g/mol
Topological Polar Surface Area:
30A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
156
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#:
N/A
Hazard Statements:
H302-H315-H319
Precautionary Statements:
P261-P302+P352-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


1-(4,6-Dimethylpyridin-2-yl)ethanone, also known as $name$, is a versatile compound widely used in chemical synthesis as a key building block. Its unique structure lends itself well to diverse applications in organic chemistry and pharmaceutical research.In chemical synthesis, $name$ serves as a valuable intermediate in the preparation of various compounds due to its reactivity and functionality. It can participate in a range of transformations, such as alkylation, acylation, and condensation reactions, allowing for the synthesis of complex organic molecules. Additionally, its presence of a pyridine ring imparts specific properties that can be leveraged in the design of novel materials and bioactive compounds.Researchers often utilize 1-(4,6-Dimethylpyridin-2-yl)ethanone to introduce specific chemical groups or functionalities into target molecules, thereby modulating their physical and chemical properties. Its versatility and synthetic utility make it an essential component in the toolkit of synthetic chemists working in various fields, including drug discovery, material science, and agrochemical development.