(4-Bromonaphthalen-1-yl)methanamine hydrochloride

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Reagent Code: #39924
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CAS Number 578029-09-1

science Other reagents with same CAS 578029-09-1

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Weight 272.5800 g/mol
Formula C₁₁H₁₁BrClN
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MDL Number MFCD08706223
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This compound is primarily utilized in organic synthesis and pharmaceutical research. It serves as a key intermediate in the development of various biologically active molecules, particularly in the synthesis of naphthalene-based compounds. Its structure is valuable for creating potential drug candidates targeting specific receptors or enzymes. Additionally, it is used in the study of chemical reactions involving brominated aromatic systems, aiding in the exploration of novel reaction pathways. Its hydrochloride form enhances solubility, making it suitable for use in aqueous or polar solvent-based reactions. Researchers also employ it in the design of fluorescent probes or imaging agents due to the naphthalene moiety's photophysical properties.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,701.00

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(4-Bromonaphthalen-1-yl)methanamine hydrochloride
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This compound is primarily utilized in organic synthesis and pharmaceutical research. It serves as a key intermediate in the development of various biologically active molecules, particularly in the synthesis of naphthalene-based compounds. Its structure is valuable for creating potential drug candidates targeting specific receptors or enzymes. Additionally, it is used in the study of chemical reactions involving brominated aromatic systems, aiding in the exploration of novel reaction pathways. Its hydro

This compound is primarily utilized in organic synthesis and pharmaceutical research. It serves as a key intermediate in the development of various biologically active molecules, particularly in the synthesis of naphthalene-based compounds. Its structure is valuable for creating potential drug candidates targeting specific receptors or enzymes. Additionally, it is used in the study of chemical reactions involving brominated aromatic systems, aiding in the exploration of novel reaction pathways. Its hydrochloride form enhances solubility, making it suitable for use in aqueous or polar solvent-based reactions. Researchers also employ it in the design of fluorescent probes or imaging agents due to the naphthalene moiety's photophysical properties.

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