CAS 64373-43-9
:Hexanenitrile, 5-methyl-3-oxo-
Description:
Hexanenitrile, 5-methyl-3-oxo- (CAS 64373-43-9) is an organic compound characterized by its nitrile functional group and a ketone moiety. It features a six-carbon chain with a methyl group at the fifth position and a carbonyl group at the third position, contributing to its unique chemical properties. This compound is typically a colorless to pale yellow liquid, exhibiting moderate volatility and solubility in organic solvents. Its structure allows for potential reactivity in various chemical reactions, including nucleophilic additions and condensation reactions. Hexanenitrile, 5-methyl-3-oxo- may be used in synthetic organic chemistry as an intermediate for the production of pharmaceuticals, agrochemicals, or other fine chemicals. Safety data indicates that, like many nitriles, it may be toxic and should be handled with appropriate precautions, including the use of personal protective equipment. Its stability under standard conditions makes it a useful compound in laboratory settings, although specific handling and storage guidelines should be followed to ensure safety and integrity.
Formula:C7H11NO
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Found 3 products.
5-Methyl-3-Oxohexanenitrile
CAS:Formula:C7H11NOPurity:95%Color and Shape:LiquidMolecular weight:125.16835-Methyl-3-oxohexanenitrile
CAS:<p>5-Methyl-3-oxohexanenitrile is a dialkylamino compound that has been used as a reagent in organic chemistry. It is tautomeric and can exist as both an amide and an isoxazole. The pyridine ring of 5-methyl-3-oxohexanenitrile can be either substituted with a carbamate, nitro, or alkenyl group, depending on the substitution pattern. 5-Methyl-3-oxohexanenitrile reacts with dinitrophenyl to form an N–N bond, which is then cleaved by amines in order to generate the corresponding carbamate or amide. 5-Methyl-3-oxohexanenitrile also reacts with copper to form the corresponding nitro or alkenyl group.</p>Formula:C7H11NOPurity:Min. 95%Molecular weight:125.17 g/mol
