3-phenylprop-2-yn-1-amine

≥95%

Reagent Code: #228163
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CAS Number 78168-74-8

science Other reagents with same CAS 78168-74-8

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Weight 131.18 g/mol
Formula C₉H₉N
badge Registry Numbers
MDL Number MFCD06654553
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used as a building block in organic synthesis, particularly in the preparation of pharmaceuticals and bioactive molecules. Its alkyne functionality allows participation in click chemistry reactions, such as copper-catalyzed azide-alkyne cycloaddition (CuAAC), making it valuable in drug discovery and combinatorial chemistry. The amine group enables easy conjugation with carbonyl compounds or carboxylic acid derivatives, facilitating the formation of amides, imines, or Schiff bases. It is also employed in the synthesis of propargylamine-based inhibitors of enzymes like monoamine oxidase (MAO), which are relevant in treating neurological disorders such as Parkinson’s and Alzheimer’s disease. Additionally, it serves as a precursor in the preparation of fluorescent probes and functionalized polymers due to its reactivity and structural features.

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inventory 1g
10-20 days ฿23,410.00

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3-phenylprop-2-yn-1-amine
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Used as a building block in organic synthesis, particularly in the preparation of pharmaceuticals and bioactive molecules. Its alkyne functionality allows participation in click chemistry reactions, such as copper-catalyzed azide-alkyne cycloaddition (CuAAC), making it valuable in drug discovery and combinatorial chemistry. The amine group enables easy conjugation with carbonyl compounds or carboxylic acid derivatives, facilitating the formation of amides, imines, or Schiff bases. It is also employed in

Used as a building block in organic synthesis, particularly in the preparation of pharmaceuticals and bioactive molecules. Its alkyne functionality allows participation in click chemistry reactions, such as copper-catalyzed azide-alkyne cycloaddition (CuAAC), making it valuable in drug discovery and combinatorial chemistry. The amine group enables easy conjugation with carbonyl compounds or carboxylic acid derivatives, facilitating the formation of amides, imines, or Schiff bases. It is also employed in the synthesis of propargylamine-based inhibitors of enzymes like monoamine oxidase (MAO), which are relevant in treating neurological disorders such as Parkinson’s and Alzheimer’s disease. Additionally, it serves as a precursor in the preparation of fluorescent probes and functionalized polymers due to its reactivity and structural features.

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