30561-09-2

Basic information

• Product Name: 5-nitro-2,4-dimethoxy-6-methylpyrimidine
• Synonyms: 5-nitro-2,4-dimethoxy-6-methylpyrimidine
• CAS NO: 30561-09-2
• Molecular Formula: C₇H₉N₃O₄
• Molecular Weight: 199
• Mol File: 30561-09-2.mol
• Article Data: 2

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 5-nitro-2,4-dimethoxy-6-methylpyrimidine(CAS DataBase Reference)
• NIST Chemistry Reference: 5-nitro-2,4-dimethoxy-6-methylpyrimidine(30561-09-2)
• EPA Substance Registry System: 5-nitro-2,4-dimethoxy-6-methylpyrimidine(30561-09-2)

Safety Data

• Hazardous Substances Data: 30561-09-2(Hazardous Substances Data)

Upstream product

• 13162-26-0 2,4-dichloro-6-methyl-5-nitropyrimidine 
• 124-41-4 sodium methylate 

Downstream Products

• 858268-26-5 4-nitro-benzenesulfonic acid-(2,4-dimethoxy-6-methyl-pyrimidin-5-ylamide) 
• 84538-40-9 2,4-dimethoxy-5H-pyrrolo<3,2-d>pyrimidine 
• 478165-06-9 N-(4-{(2S,4S,5R)-5-[Bis-(4-methoxy-phenyl)-phenyl-methoxymethyl]-4-hydroxy-tetrahydro-furan-2-ylmethyl}-5-formylamino-6-oxo-1,6-dihydro-pyrimidin-2-yl)-2-(4-isopropyl-phenoxy)-acetamide 
• 478165-03-6 N-{4-[4-(tert-butyl-dimethyl-silanyloxy)-5-(tert-butyl-dimethyl-silanyloxymethyl)-tetrahydro-furan-2-ylmethyl]-5-formylamino-6-oxo-1,6-dihydro-pyrimidin-2-yl}-2-(4-isopropyl-phenoxy)-acetamide 
• 478165-04-7 N-[5-Formylamino-4-((4S,5R)-4-hydroxy-5-hydroxymethyl-tetrahydro-furan-2-ylmethyl)-6-oxo-1,6-dihydro-pyrimidin-2-yl]-2-(4-isopropyl-phenoxy)-acetamide 
• 478164-98-6 2-isopropoxy-4-methoxy-5-nitro-6-[(triphenyl-λ⁵-phosphanylidene)-methyl]-pyrimidine 
• 83256-18-2 2,4-dimethoxy-6-<2-(dimethylamino)vinyl>-5-nitropyrimidine 
• 84538-45-4 5-amino-2,4-dimethoxy-6-methylpyrimidine 

Relevant articles and documents

Synthesis and structure-activity relationships of N3-pyridylpyrazinones as corticotropin-releasing factor-1 (CRF1) receptor antagonists

A series of N3-pyridylpyrazinones was investigated as corticotropin-releasing factor-1 receptor antagonists. It was observed that the binding affinity of analogues containing a pyridyl group was influenced not only by the substitution pattern on the pyridyl group, but also by the pKa of the pyridyl nitrogen. Analogues containing a novel 6-(difluoromethoxy)-2,5-dimethylpyridin-3-amine group were among the most potent N3-pyridylpyrazinones synthesized. The synthesis and SAR of N3-pyridylpyrazinones is described herein.