2-Bromo-1-fluoro-3-isothiocyanatobenzene

95%

Reagent Code: #141357
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CAS Number 364364-00-1

science Other reagents with same CAS 364364-00-1

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scatter_plot Molecular Information
Weight 232.07 g/mol
Formula C₇H₃BrFNS
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MDL Number MFCD22557657
inventory_2 Storage & Handling
Storage Room temperature, inert gas

description Product Description

Used primarily as a specialized building block in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. Its reactive isothiocyanate group enables conjugation with amines to form thiourea derivatives, which are important in medicinal chemistry for designing bioactive molecules. The presence of both bromo and fluoro substituents allows for selective cross-coupling reactions, making it valuable in the construction of complex aromatic systems. It is also employed in the synthesis of fluorescent probes and labeled compounds for biochemical research due to its ability to modify proteins and peptides through selective covalent binding.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿18,180.00
inventory 250mg
10-20 days ฿30,920.00
inventory 1g
10-20 days ฿83,460.00

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2-Bromo-1-fluoro-3-isothiocyanatobenzene
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Used primarily as a specialized building block in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. Its reactive isothiocyanate group enables conjugation with amines to form thiourea derivatives, which are important in medicinal chemistry for designing bioactive molecules. The presence of both bromo and fluoro substituents allows for selective cross-coupling reactions, making it valuable in the construction of complex aromatic systems. It is also employed in the syn

Used primarily as a specialized building block in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. Its reactive isothiocyanate group enables conjugation with amines to form thiourea derivatives, which are important in medicinal chemistry for designing bioactive molecules. The presence of both bromo and fluoro substituents allows for selective cross-coupling reactions, making it valuable in the construction of complex aromatic systems. It is also employed in the synthesis of fluorescent probes and labeled compounds for biochemical research due to its ability to modify proteins and peptides through selective covalent binding.

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