tert-Butyl (5-bromothiazol-2-yl)(methyl)carbamate

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Reagent Code: #87882
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CAS Number 1314095-64-1

science Other reagents with same CAS 1314095-64-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 293.18 g/mol
Formula C₉H₁₃BrN₂O₂S
badge Registry Numbers
MDL Number MFCD24469923
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

This compound is primarily utilized in organic synthesis and pharmaceutical research as an intermediate in the production of more complex molecules. Its structure, featuring a bromothiazole ring and a tert-butyl carbamate group, makes it valuable for constructing biologically active compounds, particularly in the development of drugs targeting various diseases. The bromine atom allows for further functionalization through cross-coupling reactions, enabling the creation of diverse chemical structures. Additionally, the thiazole moiety is often found in molecules with antimicrobial, anti-inflammatory, or anticancer properties, making this compound a key building block in medicinal chemistry. Its stability and reactivity also make it suitable for use in combinatorial chemistry and high-throughput screening processes.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿6,705.00

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tert-Butyl (5-bromothiazol-2-yl)(methyl)carbamate
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This compound is primarily utilized in organic synthesis and pharmaceutical research as an intermediate in the production of more complex molecules. Its structure, featuring a bromothiazole ring and a tert-butyl carbamate group, makes it valuable for constructing biologically active compounds, particularly in the development of drugs targeting various diseases. The bromine atom allows for further functionalization through cross-coupling reactions, enabling the creation of diverse chemical structures. Add

This compound is primarily utilized in organic synthesis and pharmaceutical research as an intermediate in the production of more complex molecules. Its structure, featuring a bromothiazole ring and a tert-butyl carbamate group, makes it valuable for constructing biologically active compounds, particularly in the development of drugs targeting various diseases. The bromine atom allows for further functionalization through cross-coupling reactions, enabling the creation of diverse chemical structures. Additionally, the thiazole moiety is often found in molecules with antimicrobial, anti-inflammatory, or anticancer properties, making this compound a key building block in medicinal chemistry. Its stability and reactivity also make it suitable for use in combinatorial chemistry and high-throughput screening processes.

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