1-(5-(Bromomethyl)-2-Nitrophenyl)Ethanone

Reagent Code: #154313
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CAS Number 99821-59-7

science Other reagents with same CAS 99821-59-7

blur_circular Chemical Specifications

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Weight 258.07 g/mol
Formula C₉H₈BrNO₃
inventory_2 Storage & Handling
Storage 2-8°C

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Used primarily as an intermediate in organic synthesis, this compound plays a key role in the preparation of pharmaceuticals and bioactive molecules. The presence of both a bromomethyl group and a nitro functionality allows for sequential functionalization—bromine acts as a leaving group for nucleophilic substitution, while the nitro group can be reduced to an amine for further derivatization. It is particularly valuable in the construction of heterocyclic compounds and in medicinal chemistry for building complex aromatic frameworks. Its reactivity makes it suitable for use in cross-coupling reactions and the development of nitro-containing analogs in drug discovery programs.

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inventory 100mg
10-20 days ฿2,590.00

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1-(5-(Bromomethyl)-2-Nitrophenyl)Ethanone
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Used primarily as an intermediate in organic synthesis, this compound plays a key role in the preparation of pharmaceuticals and bioactive molecules. The presence of both a bromomethyl group and a nitro functionality allows for sequential functionalization—bromine acts as a leaving group for nucleophilic substitution, while the nitro group can be reduced to an amine for further derivatization. It is particularly valuable in the construction of heterocyclic compounds and in medicinal chemistry for buildin

Used primarily as an intermediate in organic synthesis, this compound plays a key role in the preparation of pharmaceuticals and bioactive molecules. The presence of both a bromomethyl group and a nitro functionality allows for sequential functionalization—bromine acts as a leaving group for nucleophilic substitution, while the nitro group can be reduced to an amine for further derivatization. It is particularly valuable in the construction of heterocyclic compounds and in medicinal chemistry for building complex aromatic frameworks. Its reactivity makes it suitable for use in cross-coupling reactions and the development of nitro-containing analogs in drug discovery programs.

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