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Structure of 1414958-88-5
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This bench-stable boronate derivative integrates a reactive thiazole moiety with a primary amine handle, enabling direct conjugation in bioconjugation workflows. The hydrochloride salt enhances solubility and stability in aqueous media, facilitating efficient coupling under standard conditions.
(5-Bromothiazol-2-yl)methanamine hydrochloride serves as a versatile building block for the synthesis of thiazole-based pharmaceutical intermediates and functionalized heterocycles. Its bromine substituent enables palladium-catalyzed cross-coupling reactions, while the primary amine functionality facilitates conjugation, derivatization, and salt formation. The hydrochloride form enhances bench stability and solubility in polar solvents, supporting efficient purification and integration into multi-step synthetic sequences.
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GHS Pictogram :
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GHS No : GHS07
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Signal Word : Warning
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UN#: N/A
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Class : N/A
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Packing Group : N/A
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Hazard Statements : H302-H312-H315-H319-H332-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: