41055-93-0

Basic information

• Product Name: 1-Chloro-2-nonanone
• Synonyms: 1-Chloro-2-nonanone
• CAS NO: 41055-93-0
• Molecular Formula: C₉H₁₇ClO
• Molecular Weight: 0
• Mol File: 41055-93-0.mol

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 1-Chloro-2-nonanone(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Chloro-2-nonanone(41055-93-0)
• EPA Substance Registry System: 1-Chloro-2-nonanone(41055-93-0)

Safety Data

• Hazardous Substances Data: 41055-93-0(Hazardous Substances Data)

Usage

Uses

Used in the Food Industry:
1-Chloro-2-nonanone is used as a flavoring agent for its fruity and floral aroma, enhancing the taste and aroma of various food products.
Used in the Perfume and Fragrance Industry:
1-Chloro-2-nonanone is utilized as a key ingredient in the production of perfumes and fragrances, contributing to their unique and appealing scents.
Used in Pest Control:
1-Chloro-2-nonanone has potential applications as an insecticide, exhibiting insecticidal properties against certain pests, making it a valuable tool in pest management and control strategies.

Upstream product

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• 4776-43-6 1,1,1-trichlorononan-2-ol 
• 124-13-0 Octanal 
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Downstream Products

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• 873411-23-5 N-acetyl-sulfanilic acid-(4-heptyl-thiazol-2-ylamide) 
• 1259944-19-8 8-chloro-2-heptyl-3-hydroxyquinolin-4-(1H)-one 
• 1259944-21-2 6-hydroxy-2-heptyl-3-hydroxyquinolin-4-(1H)-one 
• 1259944-12-1 5-chloro-2-heptyl-3-hydroxyquinolin-4-(1H)-one 
• 1259944-22-3 5-fluoro-2-heptyl-3-hydroxyquinolin-4-(1H)-one 
• 1259944-14-3 6-chloro-2-heptyl-3-hydroxyquinolin-4-(1H)-one 
• 1262791-01-4 6-iodo-2-heptyl-3-hydroxyquinolin-4-(1H)-one 

Relevant articles and documents

ASPARAGINE DERIVATIVES AND METHODS OF USE THEREOF

The present invention relates to compounds of formulas (A) and (I), pharmaceutically acceptable salts thereof, and solvates of any of them, pharmaceutical compositions comprising them, methods of preparation thereof, intermediate compounds useful for the preparation thereof, and methods of treatment or prophylaxis of diseases, in particular cancer, such as colorectal cancer, using these. (A) (I)

COMPOUNDS FOR USE AS AN ANTI-BACTERIAL OR ANTI-FUNGAL AGENT AND AS A ZINC SENSOR

The present invention relates to a compound, which can be used as an anti-bacterial and/or an anti-fungal agent as well as a zinc sensor. Moreover, the present invention relates to a pharmaceutical composition comprising said compound and methods for treating bacterial or fungal infections in mammals.

AuIII-Catalyzed Formation of α-Halomethyl Ketones from Terminal Alkynes

A AuIII-catalyzed synthesis of α-halomethyl ketones from terminal alkynes was developed. This approach features excellent functional group compatibility and good yields for both aromatic and aliphatic terminal alkynes. The resulting α-halomethyl ketones were used to prepare heterocyclic indolizine structures. The plausible mechanism of the one-pot reaction is proposed.

Synthetic quinolone signal analogues inhibiting the virulence factor elastase of Pseudomonas aeruginosa

We explore the chemical space of Pseudomonas quinolone signal analogs as privileged structures and report the discovery of a thioquinolone as a potent inhibitor of the important virulence factor elastase of the human pathogen Pseudomonas aeruginosa. We provide evidence that the derivative binds to the active site zinc of elastase and additionally acts as a fluorescent zinc sensor.

Mild and efficient α-chlorination of carbonyl compounds using ammonium chloride and oxone (2KHSO5·KHSO4· K2SO4)

A simple protocol for the α-monochlorination of ketones and 1,3-dicarbonyl compounds utilizing NH4Cl as a source of chlorine and Oxone as an oxidant in methanol without catalyst is presented. The reaction proceeds at ambient temperature in yields ranging from moderate to excellent.

Microwave and flow syntheses of Pseudomonas quinolone signal (PQS) and analogues

Expedient syntheses of Pseudomonas quinolone signal (PQS) and related structural analogues using microwave and flow methods are reported.

α-chlorination of ketones with sodium chlorite, Mn(acac)3, and alumina in dichloromethane

Chlorination of a variety of aliphatic, alicyclic, and aromatic ketones with a reagent combination of NaC1O2 and Mn(acac)3 catalyst can be readily performed in dichloromethane to afford α-chloroketones in good yield under mild and neutral conditions with the aid of chromatographic neutral alumina.