Methyl3-bromo-2-nitrobenzoat

98%

Reagent Code: #213428
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CAS Number 104670-71-5

science Other reagents with same CAS 104670-71-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 2604 g/mol
Formula C₈H₆BrNO₄
badge Registry Numbers
MDL Number MFCD14697993
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. Its reactive bromo and nitro groups allow for selective substitutions, making it valuable in constructing complex aromatic compounds. Commonly employed in cross-coupling reactions such as Suzuki or Heck reactions to form carbon-carbon bonds. Also utilized in the development of dyes and functional materials where nitroaromatic scaffolds are required. Its ester group facilitates further derivatization, enabling its use in multi-step synthetic pathways.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,850.00
inventory 250mg
10-20 days ฿3,140.00
inventory 500mg
10-20 days ฿4,010.00
inventory 1g
10-20 days ฿5,860.00
inventory 5g
10-20 days ฿21,510.00

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Methyl3-bromo-2-nitrobenzoat
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Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. Its reactive bromo and nitro groups allow for selective substitutions, making it valuable in constructing complex aromatic compounds. Commonly employed in cross-coupling reactions such as Suzuki or Heck reactions to form carbon-carbon bonds. Also utilized in the development of dyes and functional materials where nitroaromatic scaffolds are required. Its ester group facilitates further deriv

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. Its reactive bromo and nitro groups allow for selective substitutions, making it valuable in constructing complex aromatic compounds. Commonly employed in cross-coupling reactions such as Suzuki or Heck reactions to form carbon-carbon bonds. Also utilized in the development of dyes and functional materials where nitroaromatic scaffolds are required. Its ester group facilitates further derivatization, enabling its use in multi-step synthetic pathways.

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