4,5-Dibromothiazole-2-carboxylic acid

95%

Reagent Code: #178436
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CAS Number 1806352-39-5

science Other reagents with same CAS 1806352-39-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 286.9292 g/mol
Formula C₄HBr₂NO₂S
inventory_2 Storage & Handling
Storage 2-8°C, Inert Gas

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 antiparasitic properties. Its structure serves as a building block in heterocyclic chemistry, enabling the construction of complex thiazole-based compounds. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to the reactivity of the carboxylic acid and bromine functionalities, allowing for further derivatization through cross-coupling reactions or amide formation. Also utilized in the preparation of fluorescent probes and functional materials where thiazole rings enhance electronic properties.

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inventory 25mg
10-20 days ฿2,850.00

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4,5-Dibromothiazole-2-carboxylic acid
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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 antiparasitic properties. Its structure serves as a building block in heterocyclic chemistry, enabling the construction of complex thiazole-based compounds. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to the reactivity of the carboxylic acid and bromine functionalities, allowing for f

Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of bioactive molecules with antimicrobial, antifungal, and antiparasitic properties. Its structure serves as a building block in heterocyclic chemistry, enabling the construction of complex thiazole-based compounds. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to the reactivity of the carboxylic acid and bromine functionalities, allowing for further derivatization through cross-coupling reactions or amide formation. Also utilized in the preparation of fluorescent probes and functional materials where thiazole rings enhance electronic properties.

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