126314-18-9

Basic information

• Product Name: 1-Butanone, 1-(4-chlorophenyl)-4-phenyl-
• CAS NO: 126314-18-9
• Molecular Formula: C16H15ClO
• Molecular Weight: 258.748
• Mol File: 126314-18-9.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 1-Butanone, 1-(4-chlorophenyl)-4-phenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Butanone, 1-(4-chlorophenyl)-4-phenyl-(126314-18-9)
• EPA Substance Registry System: 1-Butanone, 1-(4-chlorophenyl)-4-phenyl-(126314-18-9)

Safety Data

• Hazardous Substances Data: 126314-18-9(Hazardous Substances Data)

Usage

Class

Benzodiazepine (psychoactive substances)

Derivatives

Clonazepam and alprazolam (FDA-approved drugs)

Properties

Sedative, hypnotic, and anxiolytic

Availability

Commonly sold on the internet as a research chemical

Recreational use

Often used for recreational purposes

Medical approval

Not approved for medical use

Safety and efficacy

Not established

Health risks

Significant health risks and potentially harmful side effects associated with abuse

Upstream product

• 126314-17-8 1-(4-chlorophenyl)-4-phenylbutan-1-ol 
• 7484-37-9 (3-phenylpropyl)triphenylphosphonium bromide 
• 122334-37-6 4-chloro-N-methoxy-N-methylbenzamide 
• 122-01-0 4-chloro-benzoyl chloride 
• 637-59-2 1-Bromo-3-phenylpropane 
• 104-88-1 4-chlorobenzaldehyde 
• 1073-67-2 4-vinylbenzyl chloride 
• 84379-71-5 1,3-dioxoisoindolin-2-yl 3-phenylpropanoate 
• 100-42-5 styrene 
• 1777-56-6 4-chlorobenzoylmethylenetriphenylphosphorane 

Downstream Products

• 37562-71-3 4-phenyl-1-(p-chlorophenyl)-2-butanone 
• 126314-19-0 4-phenyl-1-(p-chlorophenyl)-4-butanone 
• 107487-79-6 trans-1-(4-Chlorophenyl)-4-phenylbut-2-ene-1,4-dione 

Relevant articles and documents

Metal-free visible light photoredox enables generation of carbyne equivalents via phosphonium ylide C-H activation

Carbyne, an interesting synthetic intermediate, has recently been generated from hypervalent iodine precursors via photoredox catalysis. Given the underexplored chemistry of carbyne, due to the paucity of carbyne sources, we are intrigued to discover a new source for this reactive species from classical reagents-phosphonium ylides. Our novel strategy employing phosphonium ylides in an olefin hydrocarbonation reaction features a facile approach for constructing carbon-carbon bonds through metal-free and benign reaction conditions. Moreover, the hydrocarbonation products were delivered in a highly regioselective manner.

Direct conversion of N-methoxy-N-methylamides (Weinreb amides) to ketones via a nonclassical Wittig reaction

(Chemical Equation Presented) N-Methoxy-N-methylamides (Weinreb amides) are converted efficiently into ketones by reaction with alkylidenetriphenylphosphoranes and in situ hydrolysis of the product.