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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-Pentanone, 4-methyl-, oxime

CC(C/C(=N\O)/C)C Request for Quotation
Chemical Name: 2-Pentanone, 4-methyl-, oxime
CAS Number: 105-44-2
Product Number: AG00343Q(AGN-PC-0JK88R)
Synonyms:
MDL No:
Molecular Formula: C6H13NO
Molecular Weight: 115.1735

Identification/Properties

Properties
BP:
68-70°C/8mmHg
Storage:
Room Temperature;
Refractive Index:
0.880

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


4-Methyl-2-pentanone oxime is a versatile compound widely used in chemical synthesis as a building block for creating various organic molecules. With its unique structural properties, this oxime plays a crucial role in the development of pharmaceuticals, agrochemicals, and specialty chemicals.One of the key applications of 4-Methyl-2-pentanone oxime is in the synthesis of heterocyclic compounds, which are essential in drug discovery and development. By utilizing this oxime as a starting material, chemists can efficiently access a diverse range of heterocycles that exhibit biological activity and therapeutic potential.Additionally, 4-Methyl-2-pentanone oxime is utilized in the preparation of complex organic molecules through various chemical transformations such as condensation reactions, oxidation, and reduction processes. Its strategic placement within a molecule can enable the introduction of specific functional groups or stereochemical elements, allowing for precise control over the final compound's properties.Furthermore, this oxime can serve as a protecting group in organic synthesis, safeguarding sensitive functional groups from undesired reactions during complex chemical transformations. By selectively masking reactive sites with 4-Methyl-2-pentanone oxime, chemists can achieve greater synthetic efficiency and enhance the overall yield of desired products.Overall, the strategic utility of 4-Methyl-2-pentanone oxime in chemical synthesis highlights its significance as a valuable tool for constructing intricate organic molecules with tailored properties and functionalities.