19182-82-2

Basic information

• Product Name: 1H-Imidazole, 2-methyl-1,4-dinitro-
• CAS NO: 19182-82-2
• Molecular Formula: C4H4N4O4
• Molecular Weight: 172.1
• Mol File: 19182-82-2.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 1H-Imidazole, 2-methyl-1,4-dinitro-(CAS DataBase Reference)
• NIST Chemistry Reference: 1H-Imidazole, 2-methyl-1,4-dinitro-(19182-82-2)
• EPA Substance Registry System: 1H-Imidazole, 2-methyl-1,4-dinitro-(19182-82-2)

Safety Data

• Hazardous Substances Data: 19182-82-2(Hazardous Substances Data)

Usage

Structure

1H-Imidazole, 2-methyl-1,4-dinitro-

Explanation

The compound is a derivative of imidazole, which is a five-membered ring containing nitrogen. It has a methyl group (CH3) and two nitro groups (NO2) attached to the imidazole ring.

Explanation

The compound contains an imidazole ring as its core structure, with two nitro groups and a methyl group as substituents.

Explanation

1H-Imidazole, 2-methyl-1,4-dinitrois used as a building block in the synthesis of various organic compounds, including pharmaceuticals and agrochemicals.

Explanation

The compound is known for its ability to engage in various chemical reactions, making it a versatile building block for the development of new materials and bioactive compounds.

Explanation

1H-Imidazole, 2-methyl-1,4-dinitrois a derivative of the imidazole, which is a five-membered ring compound containing nitrogen.

Explanation

The compound has a high nitrogen content due to the presence of the imidazole ring and the two nitro groups.

Explanation

Due to the presence of polar functional groups (nitro and imidazole), the compound is expected to be soluble in polar solvents such as water and alcohols.

Explanation

The compound is relatively stable under normal conditions, but it may undergo decomposition or react with other chemicals under specific conditions.

Explanation

Due to the presence of nitro groups, the compound may have explosive or toxic properties and should be handled with care.

Functional Groups

Imidazole ring, Nitro groups (NO2), Methyl group (CH3)

Applications

Organic synthesis, pharmaceuticals, agrochemicals, and other organic compounds

Chemical Reactivity

Participates in a wide range of chemical reactions

Derivative

Imidazole

Nitrogen Content

High

Solubility

Soluble in polar solvents

Stability

Relatively stable under normal conditions

Hazardous Properties

Potentially explosive or toxic

Upstream product

• 693-98-1 2-methylimidazole 

Downstream Products

• 135307-57-2 1-(3-Methoxy-phenyl)-2-methyl-4-nitro-1H-imidazole 
• 143248-04-8 3-(2-Methyl-4-nitro-imidazol-1-yl)-benzoic acid 
• 35687-42-4 2-Methyl-4-nitro-5-methoxyimidazol 
• 25023-24-9 1-Methoxycarbonylmethyl-2-methyl-4-nitro-imidazol 
• 138995-97-8 (S)-2-(2-Methyl-4-nitro-imidazol-1-yl)-propionic acid methyl ester 
• 143292-62-0 2-(2-Methyl-4-nitro-imidazol-1-yl)-propionic acid methyl ester 
• 143247-98-7 (S)-3-(4-Hydroxy-phenyl)-2-(2-methyl-4-nitro-imidazol-1-yl)-propionic acid methyl ester 
• 138995-98-9 (R)-2-(2-Methyl-4-nitro-imidazol-1-yl)-propionic acid methyl ester 
• 41384-82-1 2-methyl-4-nitro-1-phenyl-1H-imidazole 
• 149936-16-3 1-(3-chlorophenyl)-1-methyl-4-nitroimidazole 
• 132149-51-0 1-[(2R,4S,5S)-5-Hydroxymethyl-4-(2-methyl-4-nitro-imidazol-1-yl)-tetrahydro-furan-2-yl]-5-methyl-1H-pyrimidine-2,4-dione 
• 16230-87-8 1-carboxymethyl-2-methyl-4-nitroimidazole 
• 143248-09-3 3-(2-Methyl-4-nitro-imidazol-1-yl)-phenol 
• 143248-07-1 4-(2-Methyl-4-nitro-imidazol-1-yl)-benzoic acid ethyl ester 

Relevant articles and documents

Ozone-mediated Nitration of Pyrazole, Imidazole and Uracil with Nitrogen Dioxide

In the presence of ozone, pyrazole and uracil were easily N-nitrated with nitrogen dioxide in dichloromethane at 0°C to give the corresponding 1-nitro derivatives, whilst imidazole was C-nitrated in the additional presence of methanesulfonic acid as catalyst to afford the 4-nitro derivative, each product being obtained in a satisfactory yield.