(3,4-Dibromo-5-nitrophenyl)methanol

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Reagent Code: #130826
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CAS Number 2386098-53-7

science Other reagents with same CAS 2386098-53-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 310.93 g/mol
Formula C₇H₅Br₂NO₃
thermostat Physical Properties
Boiling Point 388.4±37.0 °C(Predicted)
inventory_2 Storage & Handling
Density 2.108±0.06 g/cm3(Predicted)
Storage Room temperature, seal, dry

description Product Description

Used primarily as an intermediate in organic synthesis, this compound serves in the preparation of pharmaceuticals and agrochemicals due to the presence of reactive functional groups. The hydroxyl group allows for esterification or ether formation, while the bromine atoms enable cross-coupling reactions such as Suzuki or Heck reactions. The nitro group can be reduced to an amine, facilitating the synthesis of more complex aromatic amines used in dyes and bioactive molecules. Its structural features make it valuable in the development of specialty chemicals requiring multi-step derivatization.

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inventory 1g
10-20 days ฿29,640.00

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(3,4-Dibromo-5-nitrophenyl)methanol
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Used primarily as an intermediate in organic synthesis, this compound serves in the preparation of pharmaceuticals and agrochemicals due to the presence of reactive functional groups. The hydroxyl group allows for esterification or ether formation, while the bromine atoms enable cross-coupling reactions such as Suzuki or Heck reactions. The nitro group can be reduced to an amine, facilitating the synthesis of more complex aromatic amines used in dyes and bioactive molecules. Its structural features make

Used primarily as an intermediate in organic synthesis, this compound serves in the preparation of pharmaceuticals and agrochemicals due to the presence of reactive functional groups. The hydroxyl group allows for esterification or ether formation, while the bromine atoms enable cross-coupling reactions such as Suzuki or Heck reactions. The nitro group can be reduced to an amine, facilitating the synthesis of more complex aromatic amines used in dyes and bioactive molecules. Its structural features make it valuable in the development of specialty chemicals requiring multi-step derivatization.

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