tert-butyl2-bromo-5-fluorobenzylcarbamate

95%

Reagent Code: #244361
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CAS Number 1358684-71-5

science Other reagents with same CAS 1358684-71-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 304.155 g/mol
Formula C₁₂H₁₅BrFNO₂
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of fluorinated benzylamine derivatives with biological activity. Its protected amine group allows selective reactions in multi-step organic syntheses. Commonly employed in medicinal chemistry for constructing kinase inhibitors and central nervous system agents. The tert-butyl carbamate (Boc) group ensures stability during reactions, while the bromo and fluoro substituents enable further functionalization via cross-coupling or nucleophilic substitution. Suitable for research in drug discovery and development of bioactive molecules.

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inventory 100mg
10-20 days ฿9,010.00

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tert-butyl2-bromo-5-fluorobenzylcarbamate
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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of fluorinated benzylamine derivatives with biological activity. Its protected amine group allows selective reactions in multi-step organic syntheses. Commonly employed in medicinal chemistry for constructing kinase inhibitors and central nervous system agents. The tert-butyl carbamate (Boc) group ensures stability during reactions, while the bromo and fluoro substituents enable further functionalization

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of fluorinated benzylamine derivatives with biological activity. Its protected amine group allows selective reactions in multi-step organic syntheses. Commonly employed in medicinal chemistry for constructing kinase inhibitors and central nervous system agents. The tert-butyl carbamate (Boc) group ensures stability during reactions, while the bromo and fluoro substituents enable further functionalization via cross-coupling or nucleophilic substitution. Suitable for research in drug discovery and development of bioactive molecules.

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