78589-10-3

Basic information

• Product Name: 4-CHLORO-2'-METHOXYBENZOPHENONE
• Synonyms: 4-CHLORO-2'-METHOXYBENZOPHENONE;UKRORGSYN-BB BBV-5118702
• CAS NO: 78589-10-3
• Molecular Formula: C₁₄H₁₁ClO₂
• Molecular Weight: 246.69
• Mol File: 78589-10-3.mol
• Article Data: 11

Chemical Properties

• Melting Point: 78°C
• Boiling Point: 404.2°C at 760 mmHg
• Flash Point: 170.2°C
• Appearance: /
• Density: 1.212g/cm³
• Vapor Pressure: 9.63E-07mmHg at 25°C
• Refractive Index: 1.578
• CAS DataBase Reference: 4-CHLORO-2'-METHOXYBENZOPHENONE(CAS DataBase Reference)
• NIST Chemistry Reference: 4-CHLORO-2'-METHOXYBENZOPHENONE(78589-10-3)
• EPA Substance Registry System: 4-CHLORO-2'-METHOXYBENZOPHENONE(78589-10-3)

Safety Data

• Hazardous Substances Data: 78589-10-3(Hazardous Substances Data)

Usage

Preparation

Obtained by reaction of 4-chlorobenzoyl chloride with anisole [–1630] in the presence of MoO2Cl2 (20 mol%) at reflux for 20 h (5%).

InChI:InChI=1/C14H11ClO2/c1-17-13-5-3-2-4-12(13)14(16)10-6-8-11(15)9-7-10/h2-9H,1H3

Upstream product

• 122-01-0 4-chloro-benzoyl chloride 
• 100-66-3 methoxybenzene 
• 18780-05-7 (p-chlorobenzoyl)pentamethylbenzene 
• 62706-94-9 ortho-methoxybenzyl-4-chlorobenzene 
• 104-88-1 4-chlorobenzaldehyde 
• 106-39-8 bromochlorobenzene 
• 201230-82-2 carbon monoxide 
• 5720-06-9 2-Methoxyphenylboronic acid 
• 74-11-3 para-chlorobenzoic acid 
• 77775-85-0 4-Chlorbenzoesaeure-difluorophosphorsaeure-anhydrid 

Relevant articles and documents

A kind of alkali to promote self-oxidation of diaryl alkane preparation diarylketones method (by machine translation)

The invention discloses a kind of alkali to promote self-oxidation of diaryl alkane preparation diarylketones method. The method is that the diaryl paraffins compound is dissolved in an organic solvent in the drying of, the addition of a base, in the 25 - 80o C reaction under air or oxygen atmosphere for 0.5 - 5 hours, to obtain diarylketones; said two aryl paraffins compound and alkali molar ratio of 1:1 - 1:3. The method overcomes the need in the prior art strong acid or expensive metal reagent or a strong oxidizing agent and the like, has the following advantages: 1) to oxygen as the oxidizing agent, avoids the use of strong or expensive chemical oxidizing agent; 2) transition metal-free catalyst, avoids the heavy metal ion in the product; 3) the process is simple, low cost, wide range of the substrate, friendly to the environment. The synthesis method disclosed in this invention in the preparation of diarylketones industrialization of the play an important role in the production. (by machine translation)

Facile preparation of aromatic ketones from aromatic bromides and arenes with aldehydes

Aromatic ketones were efficiently prepared in good yields by the reactions of aryl bromides with n-BuLi, followed by the reactions with aromatic aldehydes or aliphatic aldehydes and the subsequent treatment with molecular iodine and K2CO3, in a one-pot method. The same treatment of arenes, instead of aromatic bromides, also provided the corresponding aromatic ketones in good yields. Using these methods, various diaryl ketones and alkyl aryl ketones bearing electron-rich aromatics and electron-deficient aromatics could be prepared efficiently by a simple, transition-metal-free, and therefore environmentally benign experimental procedure.

Aluminum bases for the highly chemoselective preparation of aryl and heteroaryl aluminum compounds

Selective C H activation with a series of neutral aluminum trisamide bases led to a wide range of polyfunctional aryl and heteroaryl aluminum reagents. Ester and cyano groups are stable under the reaction conditions for this direct alumination, and donor