Methyl 2-fluoro-6-nitrobenzoate

95%

Reagent Code: #79182
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CAS Number 212189-78-1

science Other reagents with same CAS 212189-78-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 199.14 g/mol
Formula C₈H₆FNO₄
badge Registry Numbers
MDL Number MFCD09880026
thermostat Physical Properties
Boiling Point 282.9°C at 760 mmHg
inventory_2 Storage & Handling
Storage Room temperature, dry and sealed

description Product Description

Used primarily in organic synthesis as an intermediate for the production of more complex chemical compounds. It is particularly valuable in the pharmaceutical industry for the development of active pharmaceutical ingredients (APIs). The compound’s nitro and ester functional groups make it a versatile building block for further chemical modifications, such as reduction, hydrolysis, or substitution reactions. It is also employed in research settings for the study of nitroaromatic compounds and their reactivity. Additionally, it can serve as a precursor in the synthesis of agrochemicals and specialty chemicals.

Available Sizes & Pricing

Size Availability Unit Price Quantity
250mg
10-20 days ฿2,727.00
5g
10-20 days ฿23,526.00
1g
10-20 days ฿6,786.00
25g
10-20 days ฿85,644.00
Methyl 2-fluoro-6-nitrobenzoate
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Used primarily in organic synthesis as an intermediate for the production of more complex chemical compounds. It is particularly valuable in the pharmaceutical industry for the development of active pharmaceutical ingredients (APIs). The compound’s nitro and ester functional groups make it a versatile building block for further chemical modifications, such as reduction, hydrolysis, or substitution reactions. It is also employed in research settings for the study of nitroaromatic compounds and their react

Used primarily in organic synthesis as an intermediate for the production of more complex chemical compounds. It is particularly valuable in the pharmaceutical industry for the development of active pharmaceutical ingredients (APIs). The compound’s nitro and ester functional groups make it a versatile building block for further chemical modifications, such as reduction, hydrolysis, or substitution reactions. It is also employed in research settings for the study of nitroaromatic compounds and their reactivity. Additionally, it can serve as a precursor in the synthesis of agrochemicals and specialty chemicals.

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