4-Bromo-2-nitrophenylhydrazine hydrochloride

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Reagent Code: #140688
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CAS Number 100032-79-9

science Other reagents with same CAS 100032-79-9

blur_circular Chemical Specifications

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Weight 268.50 g/mol
Formula C₆H₇BrClN₃O₂
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MDL Number MFCD09260482
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as an intermediate in organic synthesis, particularly in the preparation of heterocyclic compounds and pharmaceuticals. It serves as a derivatizing agent for carbonyl compounds, aiding in the identification and characterization of aldehydes and ketones through hydrazone formation. Also employed in the development of dyes and agrochemicals due to its reactive functional groups. Its bromo and nitro substituents allow for further functionalization via cross-coupling reactions or reduction, making it valuable in multi-step synthetic routes.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿920.00
inventory 1g
10-20 days ฿3,480.00
inventory 5g
10-20 days ฿16,000.00

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4-Bromo-2-nitrophenylhydrazine hydrochloride
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Used as an intermediate in organic synthesis, particularly in the preparation of heterocyclic compounds and pharmaceuticals. It serves as a derivatizing agent for carbonyl compounds, aiding in the identification and characterization of aldehydes and ketones through hydrazone formation. Also employed in the development of dyes and agrochemicals due to its reactive functional groups. Its bromo and nitro substituents allow for further functionalization via cross-coupling reactions or reduction, making it va

Used as an intermediate in organic synthesis, particularly in the preparation of heterocyclic compounds and pharmaceuticals. It serves as a derivatizing agent for carbonyl compounds, aiding in the identification and characterization of aldehydes and ketones through hydrazone formation. Also employed in the development of dyes and agrochemicals due to its reactive functional groups. Its bromo and nitro substituents allow for further functionalization via cross-coupling reactions or reduction, making it valuable in multi-step synthetic routes.

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