7-Bromobenzo[d]oxazol-2-amine

98%

Reagent Code: #148746
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CAS Number 1211527-07-9

science Other reagents with same CAS 1211527-07-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 213.03 g/mol
Formula C₇H₅BrN₂O
badge Registry Numbers
MDL Number MFCD19375775
inventory_2 Storage & Handling
Storage 2-8°C, dry and sealed from light

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of bioactive molecules with antimicrobial, antifungal, and anticancer properties. Its structure serves as a building block in heterocyclic chemistry, enabling the construction of more complex benzoxazole derivatives. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to the bromine atom facilitating further functionalization via cross-coupling reactions such as Suzuki or Buchwald-Hartwig aminations. Also applied in the preparation of fluorescent probes and optoelectronic materials owing to the inherent photophysical properties of the benzoxazole core.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,010.00
inventory 250mg
10-20 days ฿3,290.00
inventory 1g
10-20 days ฿10,150.00
inventory 5g
10-20 days ฿38,460.00

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7-Bromobenzo[d]oxazol-2-amine
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Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of bioactive molecules with antimicrobial, antifungal, and anticancer properties. Its structure serves as a building block in heterocyclic chemistry, enabling the construction of more complex benzoxazole derivatives. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to the bromine atom facilitating further functionalization via cross-coupling react

Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of bioactive molecules with antimicrobial, antifungal, and anticancer properties. Its structure serves as a building block in heterocyclic chemistry, enabling the construction of more complex benzoxazole derivatives. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to the bromine atom facilitating further functionalization via cross-coupling reactions such as Suzuki or Buchwald-Hartwig aminations. Also applied in the preparation of fluorescent probes and optoelectronic materials owing to the inherent photophysical properties of the benzoxazole core.

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