2-Methylpropan-2-amine (S)-3,3-dimethyl-2-((((1R,2R)-2-(pent-4-yn-1-yl)cyclopropoxy)carbonyl)amino)butanoate

• CAT Number: L018229
• CAS Number: 1425038-21-6
• Molecular Formula: C19H34N2O4
• Molecular Weight: 354.51
• Purity: ≥95%
• IUPAC Name: (2S)-3,3-dimethyl-2-[[(1R,2R)-2-pent-4-ynylcyclopropyl]oxycarbonylamino]butanoic acid;2-methylpropan-2-amine
• InChI: InChI=1S/C15H23NO4.C4H11N/c1-5-6-7-8-10-9-11(10)20-14(19)16-12(13(17)18)15(2,3)4;1-4(2,3)5/h1,10-12H,6-9H2,2-4H3,(H,16,19)(H,17,18);5H2,1-3H3/t10-,11-,12-;/m1./s1
• InChIKey: YWWBXQRMMYKIGX-AUYLJXNTSA-N
• SMILES: CC(C)(C)[C@@H](C(=O)O)NC(=O)O[C@@H]1C[C@H]1CCCC#C.CC(C)(C)N

2-Methylpropan-2-amine (S)-3,3-dimethyl-2-((((1R,2R)-2-(pent-4-yn-1-yl)cyclopropoxy)carbonyl)amino)butanoate(CAT: L018229) is a complex, high-purity compound utilized in advanced pharmaceutical and chemical research. Featuring a unique cyclopropoxy-carbonyl functional group, an alkyne chain, and a butanoate ester, it is an essential intermediate in synthesizing bioactive molecules, including pharmaceuticals and enzyme inhibitors. Its stereochemically defined structure enhances its utility in asymmetric synthesis, enabling precise exploration of structure-activity relationships. This compound’s reactivity allows for diverse chemical transformations, making it a critical tool for researchers developing novel compounds in medicinal chemistry and synthetic biology.