Description

CID 134348016 ((2S,3R)-2-(((S)-tert-Butylsulfinyl)amino)-3-methylpent-4-enoic acid) is a high-purity, chiral sulfinyl compound designed for advanced research and pharmaceutical applications. With the molecular formula C₁₀H₁₉NO₃S and CAS number 1461641-97-3, this specialized chemical serves as a critical intermediate in asymmetric synthesis and medicinal chemistry. Its stereochemically defined structure ((2S,3R)-configuration) ensures precise reactivity in enantioselective transformations, making it invaluable for the development of novel therapeutics and bioactive molecules. Packaged under strict quality control, our product guarantees ≥95% purity (HPLC) and is supplied as a crystalline solid with verified spectral data (NMR, MS). Store at 2-8°C under inert conditions for optimal stability.

Properties

• CAS Number: 1461641-97-3
• Complexity: 270
• IUPAC Name: (2S,3R)-2-[[(S)-tert-butylsulfinyl]amino]-3-methyl-pent-4-enoic acid
• InChI: InChI=1S/C10H19NO3S/c1-6-7(2)8(9(12)13)11-15(14)10(3,4)5/h6-8,11H,1H2,2-5H3,(H,12,13)/t7-,8+,15+/m1/s1
• InChI Key: LKFAJBSAIXZFTJ-KUTMEBCESA-N
• Exact Mass: 233.10856464
• Molecular Formula: C10H19NO3S
• Molecular Weight: 233.33
• SMILES: C[C@H](C=C)[C@@H](C(=O)O)N[S@@](=O)C(C)(C)C
• Topological: 85.6
• Monoisotopic Mass: 233.10856464
• Synonyms: 1461641-97-3, (2S,3R)-2-(((S)-tert-Butylsulfinyl)amino)-3-methylpent-4-enoic acid, MFCD32876918, (2S,3R)-2-[[(S)-tert-butylsulfinyl]amino]-3-methylpent-4-enoic acid, DB-154339, F71453, 4-Pentenoic acid,2-[[(s)-(1,1-dimethylethyl)sulfinyl]amino]-3-methyl-,(2s,3r)-

CID 134348016 is primarily employed as a chiral building block in the synthesis of biologically active compounds, particularly in asymmetric C-C bond-forming reactions. Its tert-butylsulfinyl group acts as a highly effective chiral auxiliary, enabling stereocontrol in the preparation of complex pharmaceutical intermediates. Researchers utilize this compound in the development of enzyme inhibitors, peptidomimetics, and other small-molecule therapeutics requiring defined stereochemistry. Additionally, it serves as a precursor for advanced ligands in catalytic systems.

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