16107-87-2

Basic information

• Product Name: 6-methyl-2,3-di-p-tolylquinoxaline
• Synonyms: 6-methyl-2,3-di-p-tolylquinoxaline
• CAS NO: 16107-87-2
• Molecular Weight: 324.425
• Mol File: 16107-87-2.mol

Chemical Properties

• CAS DataBase Reference: 6-methyl-2,3-di-p-tolylquinoxaline(CAS DataBase Reference)
• NIST Chemistry Reference: 6-methyl-2,3-di-p-tolylquinoxaline(16107-87-2)
• EPA Substance Registry System: 6-methyl-2,3-di-p-tolylquinoxaline(16107-87-2)

Safety Data

• Hazardous Substances Data: 16107-87-2(Hazardous Substances Data)

Upstream product

• 1218-89-9 4,4'-dimethylbenzoin 
• 5173-28-4 1,2-di-p-tolylethane-1,2-diol 
• 89-62-3 4-methyl-2-nitroaniline 
• 496-72-0 4-methyl-1,2-diaminobenzene 
• 3457-48-5 1,2-di(4-methylphenyl)-1,2-ethanedione 

Relevant articles and documents

Room temperature facile synthesis of quinoxalines catalyzed by amidosulfonic acid

(Chemical Equation Presented) Amidosulfonic acid NH2-SO 3H catalyzed direct condensations of o-phenylenediamines with α-diketones at room temperature in organic solvents to afford quinoxalines in excellent yields. The amidosulfonic acid as a solid acid catalyst in this preparation was efficient and recoverable.

Tungstophosphoric acid/mesoporous silicas as suitable catalysts in quinoxaline synthesis

Quinoxalines and their derivatives are of great value in the chemical and biological sciences. These compounds are found in dyes, agrochemicals, and are used as building blocks of drugs for the treatment of different diseases. Quinoxalines and their deriv

In water organic synthesis: Introducing itaconic acid as a recyclable acidic promoter for efficient and scalable synthesis of quinoxaline derivatives at room temperature

Substituted quinoxaline derivatives are traditionally synthesized by co-condensation of various starting materials. Herein, we describe a novel environmentally benign in water synthetic route for the synthesis of structurally and electronically diverse ninety quinoxalines with readily available substituted o-phenylenediamine and 1,2-diketones using cheap and biodegradable itaconic acid as a mild acid promotor in 1 hours. The reaction is performed at room temperature, which proceeds through cyclo-condensation reaction followed by obtaining the aforesaid nitrogen-containing heterocyclic adducts without performing the column chromatography up to 96% total yields. The simplicity, high efficiency, and reusable of the catalyst merits this reaction condition as “green synthesis” which enables it to be useful in synthetic transformations upto gram scale level.

Efficient and sustainable Co3O4 nanocages based nickel catalyst: A suitable platform for the synthesis of quinoxaline derivatives

Engineered nanocages have emerged at the forefront of nanomaterial investigation as they possess tremendous potential to boost key chemical processes owing to their hollow architectures that can help in achieving high reactivity. With an intention to make profitable use of their morphological features guided chemical activity, we developed dispersable Co3O4 nanocages decorated with nickel nanoparticles for accessing a broad spectrum of pharmaceutically and biologically active N-heterocyclic quinoxaline nuclei using α-dicarbonyls and 1,2-diamines as precursor reagents. For designing Co3O4 nanocages, we employed a simple and scalable method involving Kirkendall effect in which thermal decomposition of Co3[Co(CN)6]2 was carried out thereafter, nanocages were loaded with Ni nanoparticles to obtain the final Ni@Co3O4 catalyst. Results revealed that Ni@Co3O4 catalyst possesses immense potential to accelerate condensation of diamines and di-carbonyls in absence of any additives under mild reaction conditions. The superior catalytic efficiency has been attributed to the hollow architecture of the nanocatalyst comprising of abundant catalytic sites. This protocol exhibits several remarkable attributes such as mild reaction conditions outstanding functional group tolerance, high yield, immense durability and reusability for six subsequent runs.

Synthesis method of quinoxaline heterocyclic derivative

The invention discloses a synthesis method of a quinoxaline heterocyclic derivative. An intermolecular redox reaction and a condensation cyclization reaction are carried out on an o-nitroaniline compound and an o-diol compound under the action of a water-soluble alkali to prepare the quinoxaline heterocyclic derivative in one step. Expensive transition metal catalysts and ligands do not need to beused, the water-soluble alkali is used as an accelerant and can be removed in a water washing manner, so that the product has no transition metal residue, the product is easy to separate, the recovery rate is high, and the method is simple in condition, easy to operate and low in equipment requirement; and the water-soluble alkali is used as the accelerant, so the unique byproduct is water, the atom economy is high, and the method has good research and industrial application prospects.

A green solid acid catalyst 12-tungstophosphoric acid H3[PW12O40] supported on g-C3N4 for synthesis of quinoxalines

A green Keggin-type heteropoly-12-tungstophosphoric acid, (H3[PW12O40].12H2O) supported on graphitic carbon nitride g-C3N4 (HPW/g-C3N4-40), was developed for one-pot s

[BBSA-DBN][HSO4]: a novel –SO3H functionalized Bronsted acidic ionic liquid for easy access of quinoxalines

Abstract: A novel –SO3H difunctionalized Bronsted acidic ionic liquid (BAIL) 1, 5-bis (butanesulphonic acid)-diazobicyclo [4,3,0] non-5-enium hydrogen sulphate [BBSA-DBN][HSO4] is introduced for efficient synthesis of quinoxalines vi

Dowex 50W: Mild efficient reusable heterogeneous catalyst for synthesis of quinoxaline derivatives in aqueous medium

An efficient, simple and eco-friendly procedure is reported in presence of heterogeneous Dowex 50W catalyst in aqueous medium under refluxing condition to produce quinoxaline derivatives. Catalyst has participated in condensation reaction between 1,2-diamines and various aromatic 1,2-diketones smoothly with excellent yield of the products in short reaction times. Dowex 50W was used more than five times in this reaction separately and showed an excellent recyclability throughout the reaction.(figure presented).

Phosphine free Mn-complex catalysed dehydrogenative C-C and C-heteroatom bond formation: A sustainable approach to synthesize quinoxaline, pyrazine, benzothiazole and quinoline derivatives

Herein the first sustainable synthesis of quinoxalines, pyrazines and benzothiazoles catalysed by a phosphine free Mn(i) complex via acceptorless dehydrogenative coupling (ADC) is reported. This method is also applied successfully to synthesize quinolines via the dehydrogenation (removal of H2) and condensation (removal of H2O) reaction between 2-aminobenzyl alcohols and secondary alcohols.

PTSA-catalyzed one-pot synthesis of quinoxalines using DMSO as the oxidant

An efficient p-toluene sulfonic acid–catalyzed, one-pot, two-step oxidative system for cyclization of o-diaminobenzene with 1,2-diaryl-2-hydroxyethanone to quinoxalines was described. A nontoxic, readily available oxidant, dimethylsulfoxide (DMSO), was applied in this process. A broad range of substrates was applied to this method, and target compounds were obtained with good yields.