3-Bromo-4-methoxy-5-nitro-benzoic acid methyl ester

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Reagent Code: #45240
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CAS Number 40258-73-9

science Other reagents with same CAS 40258-73-9

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Weight 290.0675 g/mol
Formula C₉H₈BrNO₅
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MDL Number MFCD09881752
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Used primarily in organic synthesis, this compound serves as an intermediate in the production of pharmaceuticals and agrochemicals. Its structure, featuring bromo, methoxy, and nitro groups, makes it a versatile building block for constructing more complex molecules. It is particularly valuable in the development of active pharmaceutical ingredients (APIs) where specific functional groups are required for biological activity. Additionally, it finds application in research laboratories for studying reaction mechanisms and developing new synthetic methodologies. Its ester group allows for further chemical modifications, making it a key component in the synthesis of fine chemicals and specialty materials.

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inventory 100mg
10-20 days ฿972.00

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3-Bromo-4-methoxy-5-nitro-benzoic acid methyl ester
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Used primarily in organic synthesis, this compound serves as an intermediate in the production of pharmaceuticals and agrochemicals. Its structure, featuring bromo, methoxy, and nitro groups, makes it a versatile building block for constructing more complex molecules. It is particularly valuable in the development of active pharmaceutical ingredients (APIs) where specific functional groups are required for biological activity. Additionally, it finds application in research laboratories for studying react

Used primarily in organic synthesis, this compound serves as an intermediate in the production of pharmaceuticals and agrochemicals. Its structure, featuring bromo, methoxy, and nitro groups, makes it a versatile building block for constructing more complex molecules. It is particularly valuable in the development of active pharmaceutical ingredients (APIs) where specific functional groups are required for biological activity. Additionally, it finds application in research laboratories for studying reaction mechanisms and developing new synthetic methodologies. Its ester group allows for further chemical modifications, making it a key component in the synthesis of fine chemicals and specialty materials.

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