4-Bromo-2-methylphenylisocyanate

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Reagent Code: #152850
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CAS Number 1591-98-6

science Other reagents with same CAS 1591-98-6

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Weight 212.05 g/mol
Formula C₈H₆BrNO
badge Registry Numbers
MDL Number MFCD00037039
inventory_2 Storage & Handling
Storage 2-8°C, Inert Gas

description Product Description

Used primarily as an intermediate in the synthesis of pharmaceuticals and agrochemicals. Its reactivity allows for the formation of urea and urethane derivatives, which are key structural motifs in bioactive molecules. Commonly employed in the development of herbicides and fungicides due to its ability to modify molecular activity in target compounds. Also utilized in medicinal chemistry for constructing small molecule inhibitors, particularly in research targeting enzyme modulation. The bromine substituent enables further functionalization via cross-coupling reactions, enhancing its utility in complex molecule assembly.

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inventory 1g
10-20 days ฿950.00

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4-Bromo-2-methylphenylisocyanate
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Used primarily as an intermediate in the synthesis of pharmaceuticals and agrochemicals. Its reactivity allows for the formation of urea and urethane derivatives, which are key structural motifs in bioactive molecules. Commonly employed in the development of herbicides and fungicides due to its ability to modify molecular activity in target compounds. Also utilized in medicinal chemistry for constructing small molecule inhibitors, particularly in research targeting enzyme modulation. The bromine substitu

Used primarily as an intermediate in the synthesis of pharmaceuticals and agrochemicals. Its reactivity allows for the formation of urea and urethane derivatives, which are key structural motifs in bioactive molecules. Commonly employed in the development of herbicides and fungicides due to its ability to modify molecular activity in target compounds. Also utilized in medicinal chemistry for constructing small molecule inhibitors, particularly in research targeting enzyme modulation. The bromine substituent enables further functionalization via cross-coupling reactions, enhancing its utility in complex molecule assembly.

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