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

General 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 used in the synthesis of various pharmaceuticals and agrochemicals. It is also used in the production of dyes and fragrances. The compound may also have potential applications as a reagent in organic chemistry reactions. However, it is important to handle this chemical 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 
• 4481-64-5 (4-ethyl-phenacyl)-methyl-malonic acid 
• 86490-97-3 4-(4-ethyl-phenyl)-2-methyl-4-oxo-butyric acid 
• 6097-24-1 1-(4-ethylphenyl)-2-thiocyanatoethan-1-one 
• 1253787-95-9 2-morpholino-2-(cyclohexen-1-yl)-4'-ethylacetophenone 
• 937-30-4 4-ethylacetophenone 
• 14387-10-1 (4-ethyl-phenyl)-acetic 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 

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.