2,4-Dichloro-5-fluorobenzyl bromide

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Reagent Code: #40781
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CAS Number 261763-27-3

science Other reagents with same CAS 261763-27-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 257.92 g/mol
Formula C₇H₄BrCl₂F
badge Registry Numbers
MDL Number MFCD01631381
thermostat Physical Properties
Boiling Point 94°C/1mm
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as an intermediate in the synthesis of various pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) for therapeutic drugs. It plays a role in the production of compounds with potential anti-inflammatory, antiviral, or anticancer properties. Additionally, it is employed in organic chemistry research for constructing complex molecules through reactions like nucleophilic substitution or cross-coupling. Its halogenated structure makes it valuable for introducing specific functional groups into target molecules, aiding in the development of novel chemical entities.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿8,838.00
inventory 5g
10-20 days ฿27,288.00

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2,4-Dichloro-5-fluorobenzyl bromide
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Used as an intermediate in the synthesis of various pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) for therapeutic drugs. It plays a role in the production of compounds with potential anti-inflammatory, antiviral, or anticancer properties. Additionally, it is employed in organic chemistry research for constructing complex molecules through reactions like nucleophilic substitution or cross-coupling. Its halogenated structure makes it valuable for introducing s

Used as an intermediate in the synthesis of various pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) for therapeutic drugs. It plays a role in the production of compounds with potential anti-inflammatory, antiviral, or anticancer properties. Additionally, it is employed in organic chemistry research for constructing complex molecules through reactions like nucleophilic substitution or cross-coupling. Its halogenated structure makes it valuable for introducing specific functional groups into target molecules, aiding in the development of novel chemical entities.

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