3-(Bromomethyl)-1-Methylpyrrolidine Hydrobromide

98%

Reagent Code: #154138
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CAS Number 1390654-77-9

science Other reagents with same CAS 1390654-77-9

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Weight 258.98 g/mol
Formula C₆H₁₃Br₂N
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Storage Room temperature

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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) where pyrrolidine derivatives are required. Its reactivity allows for the introduction of the pyrrolidine ring into larger molecules, facilitating the creation of compounds with biological activity. Commonly employed in medicinal chemistry for the preparation of neuroactive agents and receptor ligands. Also utilized in the production of agrochemicals and specialty chemicals requiring functionalized nitrogen heterocycles. The presence of the bromomethyl group enables alkylation reactions, making it valuable in organic synthesis routes.

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inventory 1g
10-20 days ฿27,740.00

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3-(Bromomethyl)-1-Methylpyrrolidine Hydrobromide
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) where pyrrolidine derivatives are required. Its reactivity allows for the introduction of the pyrrolidine ring into larger molecules, facilitating the creation of compounds with biological activity. Commonly employed in medicinal chemistry for the preparation of neuroactive agents and receptor ligands. Also utilized in the production of agrochemicals and specialty chemi

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) where pyrrolidine derivatives are required. Its reactivity allows for the introduction of the pyrrolidine ring into larger molecules, facilitating the creation of compounds with biological activity. Commonly employed in medicinal chemistry for the preparation of neuroactive agents and receptor ligands. Also utilized in the production of agrochemicals and specialty chemicals requiring functionalized nitrogen heterocycles. The presence of the bromomethyl group enables alkylation reactions, making it valuable in organic synthesis routes.

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