(2-Bromothiazol-5-yl)methanamine hydrochloride

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Reagent Code: #36414
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CAS Number 1001413-46-2

science Other reagents with same CAS 1001413-46-2

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Weight 229.5300 g/mol
Formula C₄H₆BrClN₂S
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MDL Number MFCD08143030
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(2-Bromothiazol-5-yl)methanamine hydrochloride is primarily utilized in organic synthesis and pharmaceutical research. It serves as a key intermediate in the development of various biologically active compounds, particularly in the synthesis of thiazole derivatives. These derivatives are often explored for their potential therapeutic applications, including antimicrobial, antiviral, and anticancer properties. The compound's structure, featuring a bromothiazole moiety, makes it valuable for constructing complex molecules in drug discovery programs. Additionally, it is employed in the preparation of ligands for catalytic processes and in the study of structure-activity relationships (SAR) to optimize drug efficacy and selectivity.

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inventory 100mg
10-20 days ฿12,114.00

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(2-Bromothiazol-5-yl)methanamine hydrochloride
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(2-Bromothiazol-5-yl)methanamine hydrochloride is primarily utilized in organic synthesis and pharmaceutical research. It serves as a key intermediate in the development of various biologically active compounds, particularly in the synthesis of thiazole derivatives. These derivatives are often explored for their potential therapeutic applications, including antimicrobial, antiviral, and anticancer properties. The compound's structure, featuring a bromothiazole moiety, makes it valuable for constructing c

(2-Bromothiazol-5-yl)methanamine hydrochloride is primarily utilized in organic synthesis and pharmaceutical research. It serves as a key intermediate in the development of various biologically active compounds, particularly in the synthesis of thiazole derivatives. These derivatives are often explored for their potential therapeutic applications, including antimicrobial, antiviral, and anticancer properties. The compound's structure, featuring a bromothiazole moiety, makes it valuable for constructing complex molecules in drug discovery programs. Additionally, it is employed in the preparation of ligands for catalytic processes and in the study of structure-activity relationships (SAR) to optimize drug efficacy and selectivity.

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