3138-76-9

Basic information

• Product Name: Quinoxaline-2,3-dicarbaldehyde
• Synonyms: Quinoxaline-2,3-dicarbaldehyde
• CAS NO: 3138-76-9
• Molecular Formula: C₁₀H₆N₂O₂
• Molecular Weight: 186.17
• Mol File: 3138-76-9.mol
• Article Data: 4

Chemical Properties

• Appearance: /
• CAS DataBase Reference: Quinoxaline-2,3-dicarbaldehyde(CAS DataBase Reference)
• NIST Chemistry Reference: Quinoxaline-2,3-dicarbaldehyde(3138-76-9)
• EPA Substance Registry System: Quinoxaline-2,3-dicarbaldehyde(3138-76-9)

Safety Data

• Hazardous Substances Data: 3138-76-9(Hazardous Substances Data)

Upstream product

• 2379-55-7 2,3-dimethylquinoxaline 
• 17311-31-8 dioxidine 

Downstream Products

• 69334-09-4 diphenyl-7,9 oxo-8<8H>cycloheptaquinoxaline 
• 85809-32-1 dihydro-7,8 hydroxy-8 diphenyl-7,9<6H>cycloheptaquinoxaline 
• 69334-12-9 diphenyl-7,9 hydroxy-8<8H>cycloheptaquinoxaline 

Relevant articles and documents

INVESTIGATION OF THE KINETICS OF THE REDOX REACTIONS OF DIOXIDINE

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Metal- and radical-free aerobic oxidation of heteroaromatic methanes: An efficient synthesis of heteroaromatic aldehydes

A metal-free and radical-free synthesis of heteroaromatic aldehydes was developed through aerobic oxidation of methyl groups in an I2/DMSO/O2 catalytic system. Under the reaction conditions, various functional groups such as methoxy, aldehyde, ester, nitro, amide, and halo (F, Cl, Br) groups were well tolerated. The bioactive compounds like chlorchinaldin derivative and papaverine were also oxidized to the corresponding aldehydes and ketones. This reaction provided an efficient method for preparing the valuable heteroaromatic aldehydes.

A NEW METHOD FOR THE OXIDATION OF METHYL TO FORMYL GROUPS IN HETEROAROMATIC DERIVATIVES

The oxidation of α- and γ-methyl-substituted heteroaromatic bases by t-BuI/DMSO ot I2/t-BuI/DMSO systems leads to the corresponding aldehydes.