50690-09-0

Basic information

• Product Name: Ethanone, 2-chloro-1-(4-ethylphenyl)- (9CI)
• Synonyms: Ethanone, 2-chloro-1-(4-ethylphenyl)- (9CI)
• CAS NO: 50690-09-0
• Molecular Formula: C₁₀H₁₁ClO
• Molecular Weight: 182.64674
• Product Categories: ACETYLHALIDE
• Mol File: 50690-09-0.mol
• Article Data: 3

Chemical Properties

• Melting Point: 38-39 °C
• Boiling Point: 284.5°C at 760 mmHg
• Flash Point: 144.9°C
• Appearance: /
• Density: 1.105g/cm³
• Vapor Pressure: 0.00297mmHg at 25°C
• Refractive Index: 1.525
• CAS DataBase Reference: Ethanone, 2-chloro-1-(4-ethylphenyl)- (9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: Ethanone, 2-chloro-1-(4-ethylphenyl)- (9CI)(50690-09-0)
• EPA Substance Registry System: Ethanone, 2-chloro-1-(4-ethylphenyl)- (9CI)(50690-09-0)

Safety Data

• Hazardous Substances Data: 50690-09-0(Hazardous Substances Data)

Usage

Description

Ethanone, 2-chloro-1-(4-ethylphenyl)(9CI) is an organic compound with the chemical formula C10H11ClO. It is a derivative of acetophenone, a common aromatic ketone. This chemical is characterized by the presence of a chloro substituent and an ethylphenyl group attached to the carbonyl group of the ketone.

Uses

Used in Pharmaceutical Industry:
Ethanone, 2-chloro-1-(4-ethylphenyl)(9CI) is used as an intermediate in the synthesis of various pharmaceuticals. Its unique structure allows it to be a versatile building block for the development of new drugs with potential therapeutic applications.
Used in Agrochemical Industry:
Ethanone, 2-chloro-1-(4-ethylphenyl)(9CI) is also utilized in the production of agrochemicals, specifically as a precursor in the synthesis of pesticides and other agricultural chemicals. Its reactivity and structural features make it suitable for the creation of effective and targeted agrochemical products.
Used in Dyes and Fragrances Industry:
Ethanone, 2-chloro-1-(4-ethylphenyl)(9CI) is employed in the formulation of dyes and fragrances due to its aromatic properties. Its ability to impart color and scent to various products makes it a valuable component in this industry.
Used as a Reagent in Organic Chemistry:
Ethanone, 2-chloro-1-(4-ethylphenyl)(9CI) may also have potential applications as a reagent in organic chemistry reactions. Its reactivity and functional groups can be harnessed to facilitate various chemical transformations and synthesis processes.
It is important to handle Ethanone, 2-chloro-1-(4-ethylphenyl)(9CI) with caution, as it may have potential health hazards and should be used with proper safety measures.

InChI:InChI=1/C10H11ClO/c1-2-8-3-5-9(6-4-8)10(12)7-11/h3-6H,2,7H2,1H3

Upstream product

• 100-41-4 ethylbenzene 
• 79-04-9 chloroacetyl chloride 
• 937-30-4 4-ethylacetophenone 
• 40307-11-7 1-ethyl-4-ethynylbenzene 

Downstream Products

• 103323-24-6 1-(4-ethylphenyl)-2-hydroxyethan-1-one 
• 937-30-4 4-ethylacetophenone 
• 14387-10-1 (4-ethyl-phenyl)-acetic acid 
• 1253787-95-9 2-morpholino-2-(cyclohexen-1-yl)-4'-ethylacetophenone 
• 4481-64-5 (4-ethyl-phenacyl)-methyl-malonic acid 
• 86490-97-3 4-(4-ethyl-phenyl)-2-methyl-4-oxo-butyric acid 
• 120007-60-5 2-(Benzooxazol-2-ylsulfanyl)-1-(4-ethyl-phenyl)-ethanone 
• 120007-50-3 3-[2-(4-Ethyl-phenyl)-2-oxo-ethyl]-3H-benzooxazol-2-one 
• 6097-24-1 1-(4-ethylphenyl)-2-thiocyanatoethan-1-one 

Relevant articles and documents

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.

α-Chlorination of Aromatic Acetyl Derivatives with Benzyltrimethylammonium Dichloroiodate

Reaction of aromatic acetyl derivatives with benzyltrimethylammonium dichloroiodate in refluxing dichloroethane/methanol for several hours gave α-chloroacetyl derivatives in good yields.