618101-71-6

Basic information

• Product Name: 1-(3-CHLOROPHENYL)-3-(3-NITROPHENYL)-1H-PYRAZOLE-4-CARBALDEHYDE
• Synonyms: 1-(3-CHLOROPHENYL)-3-(3-NITROPHENYL)-1H-PYRAZOLE-4-CARBALDEHYDE;SALOR-INT L321214-1EA;1-(3-chlorophenyl)-3-(3-nitrophenyl)pyrazole-4-carbaldehyde
• CAS NO: 618101-71-6
• Molecular Formula: C16H10ClN3O3
• Molecular Weight: 327.72
• Mol File: 618101-71-6.mol
• Article Data: 0

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 1-(3-CHLOROPHENYL)-3-(3-NITROPHENYL)-1H-PYRAZOLE-4-CARBALDEHYDE(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(3-CHLOROPHENYL)-3-(3-NITROPHENYL)-1H-PYRAZOLE-4-CARBALDEHYDE(618101-71-6)
• EPA Substance Registry System: 1-(3-CHLOROPHENYL)-3-(3-NITROPHENYL)-1H-PYRAZOLE-4-CARBALDEHYDE(618101-71-6)

Safety Data

• Hazardous Substances Data: 618101-71-6(Hazardous Substances Data)

Usage

Chemical structure

1-(3-chlorophenyl)-3-(3-nitrophenyl)-1H-pyrazole-4-carbaldehyde is a compound with a pyrazole ring and aldehyde functional group, containing a 3-chlorophenyl group and a 3-nitrophenyl group.

Functional groups

The compound has a pyrazole ring, an aldehyde functional group, a 3-chlorophenyl group, and a 3-nitrophenyl group.

Reactivity

The presence of the nitro and chloro groups in the molecule makes it potentially reactive and useful for directing the synthesis of other substituted pyrazole compounds.

Applications

The compound is commonly used in organic synthesis and medicinal chemistry as a building block for the synthesis of various pharmaceuticals and agrochemicals.

Pharmacological and biological activities

The compound has applications in the development of new drugs, insecticides, and herbicides due to its pharmacological and biological activities.

Potential uses

The compound can be used as a starting material for the synthesis of various compounds with different biological activities, such as anti-inflammatory, anti-cancer, and anti-microbial agents.

Synthesis

The compound can be synthesized through various methods, such as condensation reactions, cross-coupling reactions, and electrophilic aromatic substitution reactions.

Stability

The compound is generally stable under normal laboratory conditions, but it should be stored in a cool, dry place and protected from light to prevent decomposition.

Safety precautions

As with any chemical, appropriate safety precautions should be taken when handling 1-(3-chlorophenyl)-3-(3-nitrophenyl)-1H-pyrazole-4-carbaldehyde, including wearing gloves, safety goggles, and a lab coat. Additionally, it should be handled in a well-ventilated area or under a fume hood to minimize exposure to vapors or dust.