2,3,6-TRIMETHYLQUINOXALINE
- Name 2,3,6-TRIMETHYLQUINOXALINE
- CAS 17635-21-1
- Purity 99%
Product Details
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1.What is the 2,3,6-TRIMETHYLQUINOXALINE ?
2,3,6-Trimethylquinoxaline, a derivative of quinoxaline, is a heterocyclic aromatic compound with the molecular formula C10H10N2. It is a yellow crystalline solid characterized by a high melting point and insolubility in water. This versatile chemical intermediate is widely used in the synthesis of various organic compounds, including pharmaceuticals, dyes, and agricultural products.
2.What is the CAS number for 2,3,6-TRIMETHYLQUINOXALINE ?
The CAS number of 2,3,6-TRIMETHYLQUINOXALINE is 17635-21-1.
3.What are another words for 2,3,6-TRIMETHYLQUINOXALINE ?
Synonyms?for?2,3,6-TRIMETHYLQUINOXALINE 17635-21-1:6-Methyl-2,3-dimethylquinoxaline;2,3,6-Trimethylquinoxaline;quinoxaline, 2,3,6-trimethyl-;
4.What is 2,3,6-TRIMETHYLQUINOXALINE (17635-21-1) used for?
Used in Pharmaceutical Industry:
2,3,6-Trimethylquinoxaline is used as a key intermediate in the synthesis of pharmaceuticals for its ability to form a wide range of useful compounds with potential therapeutic properties.
Used in Dye Industry:
In the dye industry, 2,3,6-Trimethylquinoxaline is utilized as a building block for the production of various dyes, taking advantage of its aromatic structure and reactivity.
Used in Agricultural Products:
2,3,6-Trimethylquinoxaline is employed in the development of agricultural products, such as pesticides and fertilizers, due to its potential to enhance the effectiveness and properties of these products.
Overall, 2,3,6-Trimethylquinoxaline's versatility and reactivity make it a valuable compound in multiple industries, serving as a crucial intermediate for the synthesis of a diverse array of products.
InChI:InChI=1/C11H12N2/c1-7-4-5-10-11(6-7)13-9(3)8(2)12-10/h4-6H,1-3H3
Relevant articles related to 2,3,6-TRIMETHYLQUINOXALINE:
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Article |
Source |
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In water organic synthesis: Introducing itaconic acid as a recyclable acidic promoter for efficient and scalable synthesis of quinoxaline derivatives at room temperature |
Tamuli, Kashyap J.,Nath, Shyamalendu,Bordoloi, Manobjyoti supporting information, p. 983 - 1002 (2021/02/27) |
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NaOH-Mediated Direct Synthesis of Quinoxalines from o-Nitroanilines and Alcohols via a Hydrogen-Transfer Strategy |
Wang, Yan-Bing,Shi, Linlin,Zhang, Xiaojie,Fu, Lian-Rong,Hu, Weinan,Zhang, Wenjing,Zhu, Xinju,Hao, Xin-Qi,Song, Mao-Ping , p. 947 - 958 (2021/01/14) |
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Application of a reusable Co-based nanocatalyst in alcohol dehydrogenative coupling strategy: Synthesis of quinoxaline and imine scaffolds |
Panja, Dibyajyoti,Paul, Bhaskar,Balasubramaniam, Bhuvaneshwari,Gupta, Raju K.,Kundu, Sabuj , (2020/01/21) |
5.Buy 2,3,6-TRIMETHYLQUINOXALINE with the best price .
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