13362-59-9

Basic information

• Product Name: 9-METHYLACENAPHTHO(1,2-B)-QUINOXALINE
• Synonyms: 9-METHYLACENAPHTHO(1,2-B)-QUINOXALINE
• CAS NO: 13362-59-9
• Molecular Formula: C₁₉H₁₂N₂
• Molecular Weight: 268.31
• Mol File: 13362-59-9.mol
• Article Data: 21

Chemical Properties

• Melting Point: 210-211 °C(Solv: ethanol (64-17-5))
• Boiling Point: 500.1°C at 760 mmHg
• Flash Point: 228.1°C
• Appearance: /
• Density: 1.349g/cm³
• Vapor Pressure: 1.21E-09mmHg at 25°C
• Refractive Index: 1.883
• CAS DataBase Reference: 9-METHYLACENAPHTHO(1,2-B)-QUINOXALINE(CAS DataBase Reference)
• NIST Chemistry Reference: 9-METHYLACENAPHTHO(1,2-B)-QUINOXALINE(13362-59-9)
• EPA Substance Registry System: 9-METHYLACENAPHTHO(1,2-B)-QUINOXALINE(13362-59-9)

Safety Data

• Hazardous Substances Data: 13362-59-9(Hazardous Substances Data)

Usage

InChI:InChI=1/C19H12N2/c1-11-8-9-15-16(10-11)21-19-14-7-3-5-12-4-2-6-13(17(12)14)18(19)20-15/h2-10H,1H3

Upstream product

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Relevant articles and documents

A facile synthesis of phenazine and quinoxaline derivatives using magnesium sulfate heptahydrate as a catalyst

Convenient and simple procedures for the synthesis of phenazine and quinoxaline derivatives were developed via a reaction of o-phenylenediamines and 1,2-dicarbonyl compounds. In addition, the synthesis of two new 1,4-benzodiazine derivatives and the catal

Organocatalytic combinatorial synthesis of quinazoline, quinoxaline and bis(indolyl)methanes

Aims and Objective: An efficient and practical procedure for the synthesis of heterocyclic compounds such as quinazolines, quinoxalines and bis(indolyl)methanes was developed using 3,5-bis(trifluoromethyl) phenyl ammonium hexafluorophosphate (BFPHP) as a novel organocatalyst. Materials and Methods: All of the obtained products are known compounds and identified by IR, 1HNMR, 13CNMR and melting points. Result: Various products were obtained in good to excellent yields under reaction conditions Conclusion: The BFPHP organocatalyst demonstrates a novel class of non-asymmetric organocatalysts, which has gained much attention in green chemistry.

Synthesis of benzimidazole and quinoxaline derivatives using reusable sulfonated rice husk ash (RHA-SO3H) as a green and efficient solid acid catalyst

In this work, a simple, rapid and efficient method for the preparation of benzimidazoles and quinoxalines from the condensation of o-phenylene diamines with aldehydes and/or 1,2-dicarbonyl compounds in the presence of sulfonated rice husk ash (RHA-SO3H) as an efficient green catalyst is reported. RHA-SO3H can be easily prepared using a readily available organic compound by simple modification of rice husk ash. All reactions are performed under mild reaction conditions with high to excellent yields. The method is applicable to aromatic, unsaturated and hetero aromatic aldehydes. The advantages of this method are short reaction times, milder conditions, easy work-up, solvent-free conditions and catalyst reusability.

Propylsulfonic acid functionalized nanozeolite clinoptilolite as heterogeneous catalyst for the synthesis of quinoxaline derivatives

In this work, the natural nanozeolite clinoptilolite (Nano CP) was successfully functionalized by propylsulfonic acid and applied as efficient heterogeneous catalyst for the synthesis of quinoxaline derivatives in aqueous media. The nanocatalyst was chara