30561-07-0

Basic information

• Product Name: 5-nitro-2,4-dimethoxypyrimidine
• Synonyms: 5-nitro-2,4-dimethoxypyrimidine;Pyrimidine,2,4-dimethoxy-5-nitro-;2,4- dimethoxy -5- nitrimidine
• CAS NO: 30561-07-0
• Molecular Formula: C6H7N3O4
• Molecular Weight: 185
• Mol File: 30561-07-0.mol
• Article Data: 4

Chemical Properties

• Appearance: /
• Storage Temp.: Sealed in dry,Room Temperature
• CAS DataBase Reference: 5-nitro-2,4-dimethoxypyrimidine(CAS DataBase Reference)
• NIST Chemistry Reference: 5-nitro-2,4-dimethoxypyrimidine(30561-07-0)
• EPA Substance Registry System: 5-nitro-2,4-dimethoxypyrimidine(30561-07-0)

Safety Data

• Hazardous Substances Data: 30561-07-0(Hazardous Substances Data)

Usage

General Description

5-nitro-2,4-dimethoxypyrimidine is a chemical compound with the molecular formula C6H6N4O4. It is a yellow crystalline solid with a molecular weight of 190.13 g/mol. 5-nitro-2,4-dimethoxypyrimidine is primarily used as an intermediate in the synthesis of pharmaceuticals and agricultural products. It is known for its nitro and methoxy functional groups, which make it useful in various organic reactions. Additionally, 5-nitro-2,4-dimethoxypyrimidine has been studied for its potential biological activities, including its anti-inflammatory and antifungal properties. Due to its versatile applications and potential benefits, this compound is of interest in the fields of drug development and agricultural science.

Upstream product

• 124-41-4 sodium methylate 
• 49845-33-2 2,4-Dichloro-5-nitropyrimidine 
• 67-56-1 methanol 
• 89641-18-9 2,4-dimethoxypyrimidin-5-ylboronic acid 

Downstream Products

• 14048-15-8 2,4-dimethoxypyrimidin-5-ylamine 
• 16475-85-7 1,1'-(4-hydroxy-6-methyl-1,3-phenylene)diethanone 
• 100376-12-3 4-chloro-2-(2,4-dimethoxy-pyrimidin-5-ylamino)-benzoic acid 

Relevant articles and documents

N-Nitroheterocycles: Bench-Stable Organic Reagents for Catalytic Ipso-Nitration of Aryl- And Heteroarylboronic Acids

Photocatalytic and metal-free protocols to access various aromatic and heteroaromatic nitro compounds through ipso-nitration of readily available boronic acid derivatives were developed using non-metal-based, bench-stable, and recyclable nitrating reagents. These methods are operationally simple, mild, regioselective, and possess excellent functional group compatibility, delivering desired products in up to 99% yield.

1N-ALKYL-N-ARYLPYRIMIDINAMINES AND DERIVATIVES THEREOF

The present invention provides novel compounds, compounds and pharmaceutical compositions thereof, and methods of using same in the treatment of affective disorders, anxiety, depression, post-traumatic stress disorders, eating disorders, supranuclear palsy, irritable bowel syndrome, immune suppression, Alzheimer'disease, gastrointestinal diseases, anorexia nervosa, drug and alcohol withdrawal symptoms, drug addiction, inflammatory disorders, or fertility problems. The novel compounds provided by this invention are those of formula: wherein R 1, R 3, R 4, R 5, Z, Y, V, X, X', J, K, L, and M are as defined herein.