32683-48-0

Basic information

• Product Name: 1-Methyl-3,5-dinitropyrazole
• Synonyms: 1-Methyl-3,5-dinitropyrazole;1-Methyl-3,5-dinitro-1H-pyrazole
• CAS NO: 32683-48-0
• Molecular Formula: C₄H₄N₄O₄
• Molecular Weight: 172.1
• Mol File: 32683-48-0.mol

Chemical Properties

• Boiling Point: 327.3 °C at 760 mmHg
• Flash Point: 151.7 °C
• Appearance: /
• Density: 1.83 g/cm³
• Vapor Pressure: 0.000389mmHg at 25°C
• Refractive Index: 1.708
• CAS DataBase Reference: 1-Methyl-3,5-dinitropyrazole(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Methyl-3,5-dinitropyrazole(32683-48-0)
• EPA Substance Registry System: 1-Methyl-3,5-dinitropyrazole(32683-48-0)

Safety Data

• Hazardous Substances Data: 32683-48-0(Hazardous Substances Data)

Usage

Chemical structure

A pyrazole ring with a methyl group and two nitro groups attached at positions 3 and 5.

Type of compound

Organic.

Energy content

High-energy material.

Explosive properties

Yes, potentially useful in military and industrial applications.

Sensitivity

Highly sensitive to impact, friction, and heat.

Handling precautions

Must be handled with extreme caution.

Regulation

Controlled as a hazardous chemical.

Safety measures

Strict safety measures during production, storage, and transportation.

Use and handling regulations

Subject to strict regulations and guidelines to ensure safety and prevent accidents.

InChI:InChI=1/C4H4N4O4/c1-6-4(8(11)12)2-3(5-6)7(9)10/h2H,1H3

Upstream product

• 38858-89-8 3,5-dinitro-1H-pyrazole 
• 74-88-4 methyl iodide 
• 186581-53-3 diazomethane 

Downstream Products

• 132038-70-1 5-amino-1-methyl-3-nitropyrazole 
• 132038-71-2 1,1'-dimethyl-3,3'-dinitro-5-azoxypyrazole 
• 119071-40-8 1-Methyl-3,5-dinitro-4-(tosylmethyl)pyrazol 

Relevant articles and documents

SUBSTITUTED PYRIDINES FOR THE TREATMENT OF INFLAMMATORY DISEASES

Compounds having the structure of Formula (I) or pharmaceutically acceptable isomers, racemates, hydrates, solvates or salts thereof, where A, R1, R2a, R2b, R2c and R3 are as defined herein, are usefu

COMPOUNDS AND METHODS FOR KINASE MODULATION, AND INDICATIONS THEREFOR

Compounds of Formula (I) or a pharmaceutically acceptable salt, a solvate, a tautomer, an isomer or a deuterated analog thereof, wherein A, J, R1, R2, R3, R4, R5, R6, R7, R9, X, m and n are as described herein, compositions thereof, and methods and uses thereof.

Azoles, 26. - Vicarious Nucleophilic Substitution of Hydrogen in Nitropyrazole Derivatives

4-Nitropyrazoles 1a-1c and 1g-1j react with the carbanion derived from chloromethyl p-tolyl sulfone (2) to give products of the vicarious nucleophilic substitution (VNS) of hydrogen at position 5.The presence of a second nitro group at position 3 (1c) or