(1R,2S,5R)-(-)-Menthyl (S)-p-Toluenesulfinate

• CAT Number: R031443
• CAS Number: 1517-82-4
• Molecular Formula: C₁₇H₂₆O₂S
• Molecular Weight: 294.45
• Purity: ≥95%
• Synonyms: [1R-[1α(S*),2β,5α]]-4-Methylbenzenesulfinic Acid 5-Methyl-2-(1-methylethyl)cyclohexyl Ester; (1R,3R,4S)-Menthol (-)-(S)-p-Toluenesulfinate; (S)-p-Toluenesulfinic Acid (-)-(1R,3R,4S)-p-Menth-3-yl Ester; (-)-(1R)-Menthyl (S)-toluene-4-sulfinate;?(-)-(1
• Storage: -20°C
• IUPAC Name: [(1S)-5-methyl-2-propan-2-ylcyclohexyl] 4-methylbenzenesulfinate
• InChI: InChI=1S/C17H26O2S/c1-12(2)16-10-7-14(4)11-17(16)19-20(18)15-8-5-13(3)6-9-15/h5-6,8-9,12,14,16-17H,7,10-11H2,1-4H3/t14?,16?,17-,20?/m0/s1
• InChIKey: NQICGNSARVCSGJ-UPSPKRPTSA-N
• SMILES: CC1CCC(C(C1)OS(=O)C2=CC=C(C=C2)C)C(C)C

(1R,2S,5R)-(-)-Menthyl (S)-p-toluene sulfonate (Cat No.:R031443) is a chiral chemical compound. It comprises a methyl group, an (S)-p-toluene sulfonate moiety, and exhibits stereoisomerism. This compound finds utility in asymmetric synthesis and chiral resolution. The chiral menthyl group imparts enantioselectivity, making it valuable in preparing enantiomerically enriched compounds. Its role as a chiral auxiliary contributes to creating stereochemically precise molecules. The compound’s structural features and stereoselective properties are crucial in producing optically active compounds, used in pharmaceuticals, agrochemicals, and fine chemicals, advancing the development of molecules with controlled stereochemistry and improved properties.