63376-64-7

Basic information

• Product Name: 1-[2-(3,5-dimethylphenyl)ethyl]-3,5-dimethyl-benzene
• CAS NO: 63376-64-7
• Molecular Formula: C₁₈H₂₂
• Molecular Weight: 238.373
• Mol File: 63376-64-7.mol
• Article Data: 21

Chemical Properties

• Boiling Point: 331.9°Cat760mmHg
• Flash Point: 162.8°C
• Density: 0.96g/cm³
• CAS DataBase Reference: 1-[2-(3,5-dimethylphenyl)ethyl]-3,5-dimethyl-benzene(CAS DataBase Reference)
• NIST Chemistry Reference: 1-[2-(3,5-dimethylphenyl)ethyl]-3,5-dimethyl-benzene(63376-64-7)
• EPA Substance Registry System: 1-[2-(3,5-dimethylphenyl)ethyl]-3,5-dimethyl-benzene(63376-64-7)

Safety Data

• Hazardous Substances Data: 63376-64-7(Hazardous Substances Data)

Usage

Family

Benzene family

Structure

Central benzene ring with two methyl groups and an ethyl group attached at specific positions

Usage

Organic synthesis and chemical research

Applications

Building block for the synthesis of pharmaceuticals, agrochemicals, and other fine chemicals

Importance

Significant compound in the chemical industry and research community due to its unique structure and reactivity

Upstream product

• 576-83-0 2,4,6-trimethylphenyl bromide 
• 500540-48-7 1,2-bis-(3,5-dimethyl-phenyl)-2-hydroxy-ethanone 
• 108-67-8 1,3,5-trimethyl-benzene 
• 30930-49-5 bis(2-thiophenecarbonyl) peroxide 
• 107-13-1 acrylonitrile 
• 762-04-9 phosphonic acid diethyl ester 
• 927-83-3 di-t-butyldiazene 
• 108-88-3 toluene 
• 119-61-9 benzophenone 
• 39066-43-8 4-azido-2,5,6-trifluoro-3-chloropyridine 
• 17723-18-1 4-azido-3,5-dichloro-2,6-difluoropyridine 
• 1876-22-8 di-tert-butyl diperoxyoxalate 
• 10365-94-3 1,3,5-tricyanobenzene 
• 21918-35-4 1,3-bis(3,5-dimethylphenyl)-2-propanone 

Downstream Products

• 554-95-0 benzene-1,3,5-tricarboxylic acid 

Relevant articles and documents

Synthesis of 2,4,6-trimethylphenylcalcium iodide and degradation in THF solution

(Figure Presented) Heavy Grignard reagent: Despite the low reactivity of the calcium metal and the high reactivity of the resulting Ca-C bonds, the synthesis of mesitylcalcium iodide (see structure: purple I, orange Ca, red O, gray C) succeeded at very lo

Visible-Light-Driven Self-Coupling of Methylarenes Catalyzed by Ni2P?Cd0.5Zn0.5S Nanoparticles

The Ni2P?Cd0.5Zn0.5S nanoparticles photocatalyzed self-coupling of p-xylene was reported here, and the corresponding coupling product 1,2-di-p-tolylethane was obtained. The reaction could be extended to toluene derivatives with electron-donating and electron-withdrawing substituents. Ni2P?Cd0.5Zn0.5S nanoparticles had already been characterized by XRD, ICP-AES, SEM, TEM, UV/Vis, FL, XPS. The Mott–Schottky curves of Ni2P?Cd0.5Zn0.5S were made through electrochemical methods. An active carbon free-radical was captured through ESR measurement under irradiation. The research demonstrated this photocatalytic system feasible for the self-coupling reaction of toluene derivatives.

Nondirecting Group sp3 C?H Activation for Synthesis of Bibenzyls via Homo-coupling as Catalyzed by Reduced Graphene Oxide Supported PtPd@Pt Porous Nanospheres

The use of heterogeneous bimetallic Pd-based nanocatalyst for directing the inactivated sp3 C?H coupling has been scarcely explored. This work reported the formation of symmetrical C?C bonds from the inactivated sp3 C?H bonds catalyzed by employing reduced graphene oxide supported PtPd@Pt porous nanospheres. The reaction of sp3 C?H activation proceeded under mild conditions without any solvent, ligand or directing group. It is a higher atom-, step- and cost-effectiveness strategy for developing heterogeneous catalysts in the synthesis of bibenzyls with various functional groups (e. g. aryl, alkyl, methoxyl, halogen, ester, and pyridyl). (Figure presented.).