2,5-Difluoro-1-methyl-3-nitrobenzene

98%

Reagent Code: #115388
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CAS Number 1093758-82-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 173.12 g/mol
Formula C₇H₅F₂NO₂
badge Registry Numbers
MDL Number MFCD11519028
thermostat Physical Properties
Boiling Point 243.6±35.0 °C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

This chemical is primarily utilized in organic synthesis as a building block for more complex molecules. It is often employed in the development of pharmaceuticals, where its unique structure allows for the introduction of fluorine atoms into target compounds, enhancing their biological activity and stability. Additionally, it serves as an intermediate in the production of agrochemicals, contributing to the creation of pesticides and herbicides with improved efficacy. Its nitro group also makes it valuable in dye and pigment manufacturing, where it can be used to synthesize colored compounds with specific properties. In research, it is a useful reagent for studying fluorination reactions and exploring new chemical pathways.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿1,179.00
inventory 5g
10-20 days ฿4,221.00
inventory 25g
10-20 days ฿14,715.00
2,5-Difluoro-1-methyl-3-nitrobenzene
This chemical is primarily utilized in organic synthesis as a building block for more complex molecules. It is often employed in the development of pharmaceuticals, where its unique structure allows for the introduction of fluorine atoms into target compounds, enhancing their biological activity and stability. Additionally, it serves as an intermediate in the production of agrochemicals, contributing to the creation of pesticides and herbicides with improved efficacy. Its nitro group also makes it valuable in dye and pigment manufacturing, where it can be used to synthesize colored compounds with specific properties. In research, it is a useful reagent for studying fluorination reactions and exploring new chemical pathways.
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