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13708-12-8

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13708-12-8 Usage

Description

5-Methylquinoxaline is a quinoxaline derivative in which the quinoxaline (1,4-naphthyridine) skeleton is substituted at C-5 with a methyl group. It has a burnt, roasted, nutty, roasted corn, and coffee odor. It is an amber liquid and has been identified as one of the key volatile aroma compounds in roasted almonds and roasted coffee.

Uses

Used in Flavor and Fragrance Industry:
5-Methylquinoxaline is used as a flavoring agent for its nutty, roasted, peanut, and pyrazine-like taste with a yeasty, corn-chip nuance. It is particularly useful in the creation of coffee and roasted almond flavors.
Used in Chemical Synthesis:
5-Methylquinoxaline is used as a chemical intermediate in the synthesis of various compounds, such as 1,12-diphenyl-5-methyl-1,12,12a,12b-tetrahydrobis[1,2,4]triazolo[4,3-a:3′,4′-c]quinoxaline bis-cycloadducts.
Used in Research and Development:
Due to its unique chemical properties and occurrence in roasted almonds and coffee, 5-Methylquinoxaline can be used in research and development for studying the chemical composition and aroma profiles of these products.

Check Digit Verification of cas no

The CAS Registry Mumber 13708-12-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,7,0 and 8 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 13708-12:
(7*1)+(6*3)+(5*7)+(4*0)+(3*8)+(2*1)+(1*2)=88
88 % 10 = 8
So 13708-12-8 is a valid CAS Registry Number.
InChI:InChI=1/C9H8N2/c1-7-3-2-4-8-9(7)11-6-5-10-8/h2-6H,1H3

13708-12-8 Well-known Company Product Price

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  • (Code)Product description
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  • Alfa Aesar

  • (A19300)  5-Methylquinoxaline, 98%   

  • 13708-12-8

  • 1g

  • 467.0CNY

  • Detail
  • Alfa Aesar

  • (A19300)  5-Methylquinoxaline, 98%   

  • 13708-12-8

  • 5g

  • 1513.0CNY

  • Detail
  • Aldrich

  • (272310)  5-Methylquinoxaline  98%

  • 13708-12-8

  • 272310-1G

  • 423.31CNY

  • Detail

13708-12-8SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-METHYLQUINOXALINE

1.2 Other means of identification

Product number -
Other names 5-methyl quinoxaline

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only. Food additives -> Flavoring Agents
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:13708-12-8 SDS

13708-12-8Related news

5-METHYLQUINOXALINE (cas 13708-12-8) as a versatile mono-, bi- and tridentate ligand in Palladium(II) chemistry. Crystal structures of trans-[Pd(OAc)2(N1-C8H5N2Me-5)2] and [Pd(OAc)(C,N4-CH2C8H5N2-5)(PPh3)]09/07/2019

To study the potential coordination versatility of 5-methylquinoxaline, the preparation of complexes which contain it as a mono-, bi- or tridentate ligand was carried out. On reaction with [Pd(OAc)2]3 it coordinates to the metal through its less sterically blocked nitrogen atom (N(1), distal to ...detailed

13708-12-8Relevant articles and documents

Effect of Blocked ortho-Positions on the Cyclisation of Aryl-1,4-diazabuta-1,3-dienyl Radicals

McNab, Hamish,Smith, Graeme S.

, p. 996 - 997 (1982)

Indoles are the main products from the cyclisation of (2,6-dimethylphenyl)-1,4-diazabuta-1,3-dienyl radicals, together with small amounts of quinoxalines; both ring systems arise predominantly via an intermediate spirodienyl radical.

Palladium Nanoparticles Stabilized by Metal–Carbon Covalent Bonds as an Expeditious Catalyst for the Oxidative Dehydrogenation of Nitrogen Heterocycles

Sun, Xiao-Tao,Zhu, Jie,Xia, Yun-Tao,Wu, Lei

, p. 2463 - 2466 (2017)

The first method for the dehydrogenation of nitrogen heterocycles catalyzed by a palladium nanocatalyst was developed. Carbon–metal covalent-bond-stabilized nanoparticles were found to be efficient for the dehydrogenation process in the presence of tert-butyl hydroperoxide. A variety of N-heterocycles were transformed into functionalized quinolines in medium to excellent yields in water as the solvent under mild conditions by a simple operation.

Acceptorless Dehydrogenation of N-Heterocycles and Secondary Alcohols by Ru(II)-NNC Complexes Bearing a Pyrazoyl-indolyl-pyridine Ligand

Wang, Qingfu,Chai, Huining,Yu, Zhengkun

, p. 584 - 591 (2018/03/08)

Ruthenium(II) hydride complexes bearing a pyrazolyl-(2-indol-1-yl)-pyridine ligand were synthesized and structurally characterized by NMR analysis and X-ray single crystal crystallographic determinations. These complexes efficiently catalyzed acceptorless dehydrogenation of N-heterocycles and secondary alcohols, respectively, exhibiting highly catalytic activity with a broad substrate scope. The present work has established a strategy to construct highly active transition metal complex catalysts and provides an atom-economical and environmentally benign protocol for the synthesis of aromatic N-heterocyclic compounds and ketones.

Acceptorless dehydrogenation of nitrogen heterocycles with a versatile iridium catalyst

Wu, Jianjun,Talwar, Dinesh,Johnston, Steven,Yan, Ming,Xiao, Jianliang

supporting information, p. 6983 - 6987 (2013/07/26)

Gas up: A cyclometalated iridium complex is found to catalyze the dehydrogenation of various benzofused N-heterocycles, thus releasing H 2. Driven by as low as 0.1 mol % catalyst, the reaction affords quinolines, indoles, quinoxalines, isoquinolines, and β-carbolines in high yields. Copyright

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