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CAS 60886-80-8

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(1S)-(-)-Camphorsulfonylimine

Description:
(1S)-(-)-Camphorsulfonylimine is a chiral compound characterized by its unique structure, which includes a camphor-derived backbone and a sulfonylimine functional group. This compound is typically used in asymmetric synthesis and as a reagent in organic chemistry due to its ability to facilitate enantioselective reactions. It exhibits a specific optical rotation, indicating its chiral nature, and is often employed in the preparation of various pharmaceuticals and biologically active molecules. The presence of the sulfonyl group enhances its reactivity, making it a valuable intermediate in synthetic pathways. Additionally, (1S)-(-)-Camphorsulfonylimine is known for its stability under standard laboratory conditions, although it should be handled with care due to potential reactivity with nucleophiles. Its solubility properties can vary depending on the solvent used, and it is typically stored in a cool, dry place to maintain its integrity. Overall, this compound is significant in the field of synthetic organic chemistry, particularly in the development of chiral catalysts and ligands.
Formula:C10H15NO2S
InChI:InChI=1/C10H15NO2S/c1-9(2)7-3-4-10(9)6-14(12,13)11-8(10)5-7/h7H,3-6H2,1-2H3/t7-,10-/m1/s1
SMILES:CC1(C)[C@@H]2CC[C@@]31CS(=O)(=O)N=C3C2
Synonyms:
  • (7S)-10,10-dimethyl-5-thia-4-azatricyclo-(5.2.1.0
  • Bornanesultam
  • SCamphorsulfonylimine
  • (3aS,6R)-8,8-dimethyl-4,5,6,7-tetrahydro-3a,6-methano-2,1-benzothiazole 2,2-dioxide
  • (S)-(-)-10-Camphorsulfonylimine
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