7295-50-3

Basic information

• Product Name: 1-Hexanone, 1-(4-chlorophenyl)-
• CAS NO: 7295-50-3
• Molecular Formula: C12H15ClO
• Molecular Weight: 210.704
• Mol File: 7295-50-3.mol
• Article Data: 10

Chemical Properties

• CAS DataBase Reference: 1-Hexanone, 1-(4-chlorophenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Hexanone, 1-(4-chlorophenyl)-(7295-50-3)
• EPA Substance Registry System: 1-Hexanone, 1-(4-chlorophenyl)-(7295-50-3)

Safety Data

• Hazardous Substances Data: 7295-50-3(Hazardous Substances Data)

Usage

General Description

1-Hexanone, 1-(4-chlorophenyl)-, also known as P4CP, is a chemical compound with the molecular formula C12H21ClO. It is a clear, colorless liquid with a strong, sweet odor. P4CP is commonly used as a solvent in various industrial applications, including the manufacturing of paints, coatings, adhesives, and cleaning products. It is also used as a chemical intermediate in the production of pharmaceuticals and agrochemicals. P4CP is considered to be a hazardous substance and should be handled with caution due to its potential health and environmental risks.

Upstream product

• 99-91-2 para-chloroacetophenone 
• 71-36-3 butan-1-ol 
• 17380-83-5 1-(4-chlorophenyl)cyclohexan-1-ol 
• 13856-88-7 1-(p-chlorophenyl)hexan-1-ol 
• 693-25-4 n-pentylmagnesium bromide 
• 104-88-1 4-chlorobenzaldehyde 
• 104376-24-1 (E)-1-pentenylboronic acid 
• 106-39-8 bromochlorobenzene 
• 66-25-1 hexanal 
• 122-01-0 4-chloro-benzoyl chloride 
• 3391-10-4 1-(p-chlorophenyl)ethyl alcohol 
• 21406-61-1 pentyltriphenylphosphonium bromide 
• 122334-37-6 4-chloro-N-methoxy-N-methylbenzamide 
• 142-61-0 Hexanoyl chloride 

Downstream Products

• 109248-56-8 Dipenty-<4-chlor-phenyl>-methan 
• 132104-25-7 -pentyl-<4-chlor-phenyl>-methan 
• 2001-08-3 2-bromo-1-(4-chlorophenyl)hexan-1-one 
• 107680-27-3 (2R,3R)-2-(4-Chloro-phenyl)-3-[1,2,4]triazol-1-ylmethyl-heptane-2,3-diol 
• 107680-26-2 (2R,3S)-2-(4-Chloro-phenyl)-3-[1,2,4]triazol-1-ylmethyl-heptane-2,3-diol 
• 94147-62-3 1-(4-Chloro-phenyl)-2-hydroxy-2-[1,2,4]triazol-1-ylmethyl-hexan-1-one 
• 93004-07-0 α-<4-Chlor-phenyl>-hexylamin 
• 91768-09-1 1,1-Dichlor-1-(4-chlor-phenyl)-hexan 
• 109249-68-5 Dipentyl-<4-chlor-phenyl>-carbinol 
• 38237-76-2 1-(4-aminophenyl)-hexan-1-one 

Relevant articles and documents

Preparation method of aryl ketone compound

The invention provides a preparation method of an aryl ketone compound, and belongs to the technical field of compound synthesis. The method comprises the following steps: under the action of a silver catalyst and water, carrying out reaction on aryl alkyne with a structure as shown in a formula 1 in a solvent at 60-120 DEG C for 12-48 hours, and separating and purifying a product after the reaction is finished, so as to obtain the single aryl ketone compound with a structure as shown in a formula I, the raw materials are easy to obtain, the experimental operation is simple, the yield of the prepared single aryl ketone compound is good, and gram-scale experiments can be carried out.

CARBOXY DERIVATIVES WITH ANTIINFLAMMATORY PROPERTIES

The invention relates to compounds of formula (I) and to their use in treating or preventing an inflammatory disease or a disease associated with an undesirable immune response: (I) wherein, RA1, RA2, RC and RD are as defined herein.

An Efficient α-alkylation of aromatic ketones with primary alcohols catalyzed by [cp*ircl2]2 without solvent

Aromatic ketones are directly alkylated at α position with primary alcohols at 110°C in the presence of catalytic amount of KOH and [Cp*IrCl2]2 (Cp=pentamethylcyclopentadienyl) catalyst. The reaction is carried out in the absence of any solvent or additive, which generates only water as the byproduct in theory. It is very efficient and generally completed in 10 min in good isolated yields. The reaction is believed to undergo successive hydrogen transfer and cross aldol condensation processes. Copyright