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(S)-N-Boc-3-Amino-1-butyne, often abbreviated as (S)-N-Boc-3-yn-Bu-NH2, is an organic compound that serves as a valuable building block in organic synthesis and medicinal chemistry. This compound is characterized by its molecular formula C9H17NO2 and a molecular weight of 171.24 g/mol. The N-Boc protection group in the molecule plays a crucial role in preventing unwanted side reactions, particularly with the amino group, during synthetic sequences.
As a chiral compound, (S)-N-Boc-3-Amino-1-butyne exhibits biological activity and is often used in the synthesis of pharmaceuticals and biologically active molecules. The Boc group (tert-butyloxycarbonyl) is a commonly used protecting group in organic synthesis to shield amines from unwanted reactions until they are deprotected at a later stage in a synthesis process.
This compound typically appears as a colorless to pale yellow liquid or solid, depending on the conditions. It is soluble in various organic solvents such as dichloromethane, tetrahydrofuran, and acetonitrile. The compound should be stored at low temperatures, typically between 2-8°C, to maintain its stability.