5709-95-5

Basic information

• Product Name: 2,2,8,8-Tetramethylnonane-5-one
• Synonyms: 2,2,8,8-Tetramethyl-5-nonanone;2,2,8,8-Tetramethylnonane-5-one
• CAS NO: 5709-95-5
• Molecular Formula: C₁₃H₂₆O
• Molecular Weight: 0
• Mol File: 5709-95-5.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2,2,8,8-Tetramethylnonane-5-one(CAS DataBase Reference)
• NIST Chemistry Reference: 2,2,8,8-Tetramethylnonane-5-one(5709-95-5)
• EPA Substance Registry System: 2,2,8,8-Tetramethylnonane-5-one(5709-95-5)

Safety Data

• Hazardous Substances Data: 5709-95-5(Hazardous Substances Data)

Usage

Classification

Cyclic ketone

Common uses

Fragrance ingredient in perfumes and scented products, solvent, manufacturing of other chemicals

Physical properties

Clear, colorless liquid, strong fruity odor

Safety

Relatively safe for use in consumer products when used within regulations and guidelines, harmful if ingested or inhaled in large quantities

Flammability

Highly flammable

Upstream product

• 558-37-2 tert-butylethylene 
• 2038-57-5 3-Phenylpropan-1-amine 
• 64-04-0 phenethylamine 
• 256379-28-9 N-(3-methyl-2-pyridyl)-N-[(E)-3-phenyl-2-propenyl]amine 
• 104-53-0 3-phenyl-propionaldehyde 

Relevant articles and documents

The effects of amine and acid catalysts on efficient chelation-assisted hydroacylation of alkene with aliphatic aldehyde

Efficient intermolecular hydroacylation of 1-alkene with aliphatic aldehyde was achieved using a catalyst mixture of cyclohexylamine, p-trifluoromethylbenzoic acid, Wilkinson's complex and 2-amino-3-picoline. The formation of unwanted aldol side-product w

Catalytic activation of C-H and C-C bonds of allylamines via olefin isomerization by transition metal complexes

(matrix presented) The metal-catalyzed reaction of olefins with allylamines bearing coordination sites (2-pyridyl groups) was studied. With Ru3(CO)12 as catalyst, activation of C-H bonds led to the formation of ketimines that were hydrolyzed to give asymmetric ketones. With [(C8H14)2RhCl]2, both C-H and C-C bonds were activated and symmetric ketones were formed on hydrolysis. The reaction involves double bond migration of the allylamine to form an aldimine.