Benzoic acid, 3-bromo-2-[[(1,1-dimethylethoxy)carbonyl]oxy]-6-fluoro-, 1,1-dimethylethyl ester

95%

Reagent Code: #53834
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CAS Number 1617498-11-9

science Other reagents with same CAS 1617498-11-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 391.23 g/mol
Formula C₁₆H₂₀BrFO₅
inventory_2 Storage & Handling
Storage 2-8°C, dry, sealed

description Product Description

This compound is primarily utilized in organic synthesis as an intermediate for the preparation of more complex chemical structures. Its functional groups, including the fluoro and bromo substituents, make it a versatile building block in the development of pharmaceuticals and agrochemicals. The tert-butyl ester group enhances its stability, allowing for controlled reactions in multi-step synthetic processes. Additionally, its structure is particularly useful in the synthesis of active pharmaceutical ingredients (APIs) where specific halogenated aromatic systems are required. The compound’s reactivity and selectivity make it valuable in medicinal chemistry research, particularly in designing molecules with targeted biological activity.

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inventory 100mg
10-20 days ฿41,940.00

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Benzoic acid, 3-bromo-2-[[(1,1-dimethylethoxy)carbonyl]oxy]-6-fluoro-, 1,1-dimethylethyl ester
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This compound is primarily utilized in organic synthesis as an intermediate for the preparation of more complex chemical structures. Its functional groups, including the fluoro and bromo substituents, make it a versatile building block in the development of pharmaceuticals and agrochemicals. The tert-butyl ester group enhances its stability, allowing for controlled reactions in multi-step synthetic processes. Additionally, its structure is particularly useful in the synthesis of active pharmaceutical ing

This compound is primarily utilized in organic synthesis as an intermediate for the preparation of more complex chemical structures. Its functional groups, including the fluoro and bromo substituents, make it a versatile building block in the development of pharmaceuticals and agrochemicals. The tert-butyl ester group enhances its stability, allowing for controlled reactions in multi-step synthetic processes. Additionally, its structure is particularly useful in the synthesis of active pharmaceutical ingredients (APIs) where specific halogenated aromatic systems are required. The compound’s reactivity and selectivity make it valuable in medicinal chemistry research, particularly in designing molecules with targeted biological activity.

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