2,4-Dodecadienamide, N-(2-methylpropyl)-, (2E,4E)-|24738-51-0,AngeneChemical

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Pyrimidine, 5-bromo-2-methyl-

1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide

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)-

2,4-Dodecadienamide, N-(2-methylpropyl)-, (2E,4E)-

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Chemical Name:	2,4-Dodecadienamide, N-(2-methylpropyl)-, (2E,4E)-
CAS Number:	24738-51-0
Product Number:	AG00C4FF(AGN-PC-0O8800)
Synonyms:
MDL No:
Molecular Formula:	C16H29NO
Molecular Weight:	251.40756

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Chemical Structure

Kalecide is a versatile chemical reagent that plays a crucial role in various chemical synthesis processes. Its primary application lies in its ability to act as a powerful oxidizing agent, facilitating the conversion of primary and secondary alcohols into their corresponding aldehydes and ketones, respectively. This feature makes Kalecide an indispensable tool in organic chemistry for the selective oxidation of specific functional groups, leading to efficient and controlled synthetic pathways. Additionally, Kalecide provides a convenient and cost-effective solution for the conversion of sulfides to sulfoxides or sulfones, a common transformation in organic synthesis. Its compatibility with a wide range of reaction conditions and substrates makes Kalecide a valuable asset in the laboratory for achieving desired chemical transformations with high selectivity and yield.