6135-08-6

Basic information

• Product Name: 1-(dimethylamino)hex-1-en-3-one
• CAS NO: 6135-08-6
• Molecular Formula: C₈H₁₅NO
• Molecular Weight: 141.2108
• Mol File: 6135-08-6.mol
• Article Data: 5

Chemical Properties

• Boiling Point: 208.663°C at 760 mmHg
• Flash Point: 65.193°C
• Density: 0.89g/cm³
• Vapor Pressure: 0.211mmHg at 25°C
• Refractive Index: 1.454
• CAS DataBase Reference: 1-(dimethylamino)hex-1-en-3-one(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(dimethylamino)hex-1-en-3-one(6135-08-6)
• EPA Substance Registry System: 1-(dimethylamino)hex-1-en-3-one(6135-08-6)

Safety Data

• Hazardous Substances Data: 6135-08-6(Hazardous Substances Data)

Usage

Type of compound

Ketone derivative

Structure

Six-carbon chain with a double bond and a dimethylamino group attached to the first carbon atom

Common uses

a. Flavoring agent in the food industry
b. Production of perfumes and fragrances

Aroma

Fruity and citrus-like

Potential applications

a. Pharmaceuticals
b. Organic synthesis

Safety precautions

Handle with care due to potential flammability and irritant properties

Upstream product

• 58953-13-2 (1E)-1-chlorohex-1-en-3-one 
• 124-40-3 dimethyl amine 
• 59127-76-3 1-dimethylamino-3-hexanone 
• 107-87-9 2-Pentanone 
• 20353-93-9 [3-(dimethylamino)-2-azaprop-2-en-1-ylidene]-dimethylammonium chloride 
• 20353-93-9 Gold's reagent 
• 19125-81-6 6-Dimethylamino-hexadien-(2.5)-on-⁽⁴⁾ 
• 13061-80-8 hex-4-en-1-yn-3-one 
• 4637-24-5 N,N-dimethyl-formamide dimethyl acetal 

Downstream Products

• 762-06-1 oct-5-en-4-one 
• 4643-25-8 hept-2-en-4-one 

Relevant articles and documents

ENDOPARASITIC DEPSIPEPTIDES

The present invention provides cyclic depsipeptides of Formula (1), stereoisomers thereof, and veterinary acceptable salts thereof (1) wherein each of R1, R2, R3, R4, L1, and L2, are as defined herein. The present invention also contemplates compositions and methods of treatment as an endoparasiticide with a Formula (1) compound.

Palladium-Promoted Transformation of β-Amino Ketones to Enaminones

The reaction of β-amino ketones with bis(acetonitrile)dichloropalladium(II) in the presence of triethylamine gives the corresponding enaminones regioselectively.The cyclic β-amino ketones can be converted into the corresponding exocyclic enaminones.The enaminones thus obtained are versatile synthetic intermediates.The reaction of (E)-enaminones with organocuprates gave the corresponding (E)-α,β-unsaturated ketones.

REACTION OF UBSYMMETRICAL ENOLATE ANIONS WITH GOLDS'S REAGENT

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