53525-65-8

Basic information

• Product Name: 5H,10H-DIIMIDAZO[1,5-A:1', 5'-D] PYRAZINE-5,10-DIONE
• Synonyms: SPECS AN-584/43226970;5H,10H-DIIMIDAZO[1,5-A:1', 5'-D] PYRAZINE-5,10-DIONE;DIIMIDAZO[1,5-A:1',5'-D]PYRAZINE-5,10-DIONE;Diimidazo[1,5-a:1',5'-d]pyrazine-5,10-dione, dihydrochloride;Diimidazo[1,5-a:1’,5’-d)pyrazine-5,10-dione,HCl;5H,10H-Diimidazo[1,5-A:1', 5'-D] pyrazine-5,10-dione ,98%;DiiMidazo[1,5-a:1',5'-d]pyrazine-5,10-dione, DiHCl
• CAS NO: 53525-65-8
• Molecular Formula: C₈H₄N₄O₂
• Molecular Weight: 261.06
• Product Categories: blocks;BuildingBlocks;Imidazoles;Pyridines
• Mol File: 53525-65-8.mol
• Article Data: 7

Chemical Properties

• Boiling Point: 604.5 °C at 760 mmHg
• Flash Point: 319.4 °C
• Appearance: /
• Density: 1.85 g/cm³
• Storage Temp.: 2-8°C
• CAS DataBase Reference: 5H,10H-DIIMIDAZO[1,5-A:1', 5'-D] PYRAZINE-5,10-DIONE(CAS DataBase Reference)
• NIST Chemistry Reference: 5H,10H-DIIMIDAZO[1,5-A:1', 5'-D] PYRAZINE-5,10-DIONE(53525-65-8)
• EPA Substance Registry System: 5H,10H-DIIMIDAZO[1,5-A:1', 5'-D] PYRAZINE-5,10-DIONE(53525-65-8)

Safety Data

• Hazardous Substances Data: 53525-65-8(Hazardous Substances Data)

Usage

General Description

5H,10H-Diimidazo[1,5-a:1',5'-d]pyrazine-5,10-dione is a chemical compound with a complex and bulky molecular structure. It belongs to the class of diimidazo pyrazine diones and is commonly used as a building block in the synthesis of organic compounds. 5H,10H-DIIMIDAZO[1,5-A:1', 5'-D] PYRAZINE-5,10-DIONE exhibits potential applications in the fields of pharmaceuticals, materials science, and organic synthesis due to its unique reactivity and versatility. Its specific chemical properties and reactivity make it a valuable tool for the preparation of various complex organic molecules and materials.

Upstream product

• 1072-84-0 imidazole-4-carboxylic acid 
• 61985-23-7 methyl 1-imidazolecarboxylate 
• 17325-26-7 1H-imidazole-5-carboxylic acid methyl ester 
• 13189-13-4 5-(anilinocarbonyl)imidazole 
• 56460-32-3 imidazole-4-carboxylic acid chloride 
• 1072-84-0 3H-imidazole-4-carboxylic acid 

Downstream Products

• 23785-21-9 ethyl 1H-imidazole-4-carboxylate 
• 99240-58-1 4(5)-imidazole 
• 53525-55-6 1⁽³⁾H-imidazole-4-carboxylic acid methylamide 
• 69147-97-3 N-(2-Bromophenyl)-imidazole-4⁽⁵⁾-carboxamide 
• 111074-70-5 4⁽⁵⁾-(2,4-dichlorobenzylaminocarbonyl)imidazole 
• 240815-48-9 N-(2-chloro-3-pyridinyl)-1H-imidazole-4-carboxamide 
• 240815-51-4 3H-imidazole-4-carboxylic acid (2,6-dichloro-pyridin-3-yl)-amide 
• 357647-43-9 3H-imidazole-4-carboxylic acid (4-bromo-2-fluoro-phenyl)-amide 
• 357647-44-0 3H-imidazole-4-carboxylic acid (5-bromo-2,4-difluoro-phenyl)-amide 
• 53525-55-6 1⁽³⁾H-imidazole-4-carboxylic acid methylamide 
• 1123512-68-4 N-(5-(5-(4-(difluoromethoxy)phenyl)pyrimidin-2-ylamino)-2-methylphenyl)-1H-imidazole-5-carboxamide 
• 869491-11-2 N-cyclopropyl-1H-imidazole-4-carboxamide 
• 240815-48-9 N-(2-Chloro-3-pyridinyl)-1H-imidazole-4-carboxamide 
• 240815-51-4 N-(2,6-Dichloro-3-pyridinyl)-1H-imidazole-4-carboxamide 

Relevant articles and documents

Imidazo[1,2-a]pyrazine, Imidazo[1,5-a]quinoxaline and?Pyrazolo[1,5-a]quinoxaline derivatives as IKK1 and IKK2 inhibitors

The transcription nuclear factor NF-κB plays a pivotal role in chronic and acute inflammatory diseases. Among the several and diverse strategies for inhibiting NF-κB, one of the most effective approach considered by the pharmaceutical industry seems to be

DIFLUOROALKENE DERIVATIVE, PEST CONTROL AGENT CONTAINING THE SAME, AND INTERMEDIATE THEREFOR

A difluoroalkene derivative which is sufficiently effective in controlling various pests even when used in a small dose and is highly safe for crops, natural enemies to the pests, and animals; and an intermediate for the derivative. The difluoroalkene derivative is represented by the general formula: [I] wherein L1 and L2 are the same or different and each represents oxygen or sulfur; n is an integer of 2 to 8; and Q represents a 5- to 12-membered heterocyclic group having any desired heteroatom selected among nitrogen, oxygen, and sulfur.

Synthesis of imidazo[1,5-a]quinoxalin-4(5H)-one template via a novel intramolecular cyclization process

A novel, efficient, and regiospecific method for the construction of the imidazo[1,5-a]quinoxalin-4(5H)-one template is described. The key reaction involves an intramolecular cyclization process and provides the desired products in excellent yield.