13319-70-5

Basic information

• Product Name: 5-Benzoyl-M-xylene
• Synonyms: 5-Benzoyl-M-xylene;(3,5-Dimethyl-phenyl)-phenyl-methanone
• CAS NO: 13319-70-5
• Molecular Formula: C₁₅H₁₄O
• Molecular Weight: 210.27106
• Mol File: 13319-70-5.mol
• Article Data: 29

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 5-Benzoyl-M-xylene(CAS DataBase Reference)
• NIST Chemistry Reference: 5-Benzoyl-M-xylene(13319-70-5)
• EPA Substance Registry System: 5-Benzoyl-M-xylene(13319-70-5)

Safety Data

• Hazardous Substances Data: 13319-70-5(Hazardous Substances Data)

Usage

Description

5-Benzoyl-M-xylene is an organic compound that serves as a valuable synthetic intermediate in the chemical industry. It is characterized by its unique molecular structure, which features a benzoyl group attached to a xylene molecule. This structure endows 5-Benzoyl-M-xylene with specific chemical properties that make it suitable for various applications.

Uses

5-Benzoyl-M-xylene is used as a synthetic intermediate for the production of various chemical compounds and materials. Its application reason is due to its unique molecular structure, which allows for further chemical reactions and modifications to create a wide range of products.
Used in Pharmaceutical Industry:
5-Benzoyl-M-xylene is used as a building block for the synthesis of pharmaceutical compounds. Its application reason is its ability to be modified and functionalized to create molecules with specific biological activities, making it a valuable tool in the development of new drugs.
Used in Chemical Industry:
5-Benzoyl-M-xylene is used as a starting material for the synthesis of various organic compounds, such as dyes, pigments, and polymers. Its application reason is its versatility in undergoing different chemical reactions, enabling the production of a diverse array of products with various applications.
Used in Material Science:
5-Benzoyl-M-xylene is used as a component in the development of advanced materials, such as specialty polymers and coatings. Its application reason is its compatibility with other molecules and its ability to impart specific properties to the final material, making it a useful addition to the material scientist's toolbox.

Upstream product

• 4044-60-4 2,5-dimethylbenzophenone 
• 6613-44-1 3,5-dimethylbenzoyl chloride 
• 71-43-2 benzene 
• 98-88-4 benzoyl chloride 
• 108-38-3 m-xylene 
• 7446-70-0 aluminium trichloride 
• 93-97-0 benzoic acid anhydride 
• 172975-69-8 3,5-dimethylphenyl boronic acid 
• 499-06-9 3,5-dimethylbenzoic acid 
• 98-80-6 phenylboronic acid 
• 201230-82-2 carbon monoxide 
• 22445-41-6 3,5-dimethylphenyl iodide 
• 119072-55-8 tert-butylisonitrile 
• 591-50-4 iodobenzene 

Downstream Products

• 28122-27-2 1-benzyl-3,5-dimethylbenzene 
• 13389-71-4 (3,5-dimethylphenyl)(phenyl)methanol 

Relevant articles and documents

Method for preparing aldehyde ketone compound through olefin oxidation

The invention provides a method for preparing an aldehyde ketone compound by olefin oxidation, which relates to an olefin oxidative cracking reaction in which oxygen participates. The method comprises the following specific steps: in the presence of a solvent and an oxidant, carrying out oxidative cracking on an olefin raw material to obtain a corresponding aldehyde ketone product. Compared with the traditional method, the method does not need to add any catalyst or ligand, does not need to use high-pressure oxygen, has the advantages of simple and mild reaction conditions, environment friendliness, low cost, high atom economy and the like, is wide in substrate application range and high in yield, and has a wide application prospect in the aspects of synthesis of aldehyde ketone medical intermediates and chemical raw materials.

Highly Selective and Divergent Acyl and Aryl Cross-Couplings of Amides via Ir-Catalyzed C-H Borylation/N-C(O) Activation

Herein, we demonstrate that amides can be readily coupled with nonactivated arenes via sequential Ir-catalyzed C-H borylation/N-C(O) activation. This methodology provides facile access to biaryl ketones and biaryls by the sterically controlled Ir-catalyzed C-H borylation and divergent acyl and decarbonylative amide N-C(O) and C-C activation. The methodology diverts the traditional acylation and arylation regioselectivity, allowing us to directly utilize readily available arenes and amides to produce valuable ketone and biaryl motifs.

Transition-Metal-Free Carbonylative Suzuki-Miyaura Reactions of Aryl Iodides with Arylboronic Acids Using N-Formylsaccharin as CO Surrogate

Unprecedented, high yielding, transition-metal-free carbonylative Suzuki-Miyaura reactions of aryl iodides with arylboronic acids using N-formylsaccharin as CO surrogate have been developed. Notably, this general protocol was adapted to the synthesis of the triglyceride and cholesterol regulator drug, fenofibrate, and carbon-13 labeled biaryl ketone. (Figure presented.).