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Structure of 14003-16-8
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(5-Methylfuran-2-yl)methanamine is a heterocyclic amine featuring a methyl-substituted furan ring linked to a primary amine group. This scaffold delivers enhanced solubility and stability in polar solvents, enabling efficient incorporation into bioactive molecule synthesis. The electron-rich furan system facilitates transition metal-catalyzed coupling reactions, while the pendant amine serves as a versatile handle for conjugation and derivatization.
(5-Methylfuran-2-yl)methanamine serves as a versatile building block for heterocyclic synthesis, particularly in the development of bioactive molecules and pharmaceutical intermediates. Its furan ring provides a stable, electron-rich scaffold with good bench stability and compatibility with standard functional group transformations. The primary amine enables straightforward derivatization via amidation, alkylation, or reductive amination, facilitating rapid access to diverse compound libraries. This reagent functions effectively in both solution-phase and solid-phase synthetic workflows, offering reliable yields and ease of purification.
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GHS Pictogram :
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GHS No : GHS02
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Signal Word : Danger
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UN#: 1993
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Class : 3
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Packing Group : Ⅲ
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Hazard Statements : H225-H315-H319-H335
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Precautionary Statements : P210-P233-P240-P241-P242-P243-P280-P303+P361+P353-P370+P378-P403+P235-P501
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Lot numbers can be found on the outside label of a product: