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CAS 133095-74-6

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(S)-1-TOSYLOXY-3-BUTEN-1-OL

Description:
(S)-1-Tosyloxy-3-buten-1-ol is an organic compound characterized by its functional groups and stereochemistry. It features a tosylate group, which is a sulfonate ester derived from toluenesulfonic acid, enhancing its reactivity, particularly in nucleophilic substitution reactions. The presence of a butenol structure indicates that it contains a double bond and a hydroxyl group, contributing to its potential as a versatile intermediate in organic synthesis. The compound is chiral, with the (S) configuration denoting the specific spatial arrangement of its atoms, which can influence its reactivity and interactions in biological systems. Typically, such compounds are used in the synthesis of more complex molecules, including pharmaceuticals and agrochemicals. Its solubility and stability can vary depending on the solvent and conditions, making it important to consider these factors in practical applications. Overall, (S)-1-tosyloxy-3-buten-1-ol serves as a valuable building block in organic chemistry due to its functional versatility and reactivity.
Formula:C11H14O4S
InChI:InChI=1/C11H14O4S/c1-3-10(12)8-15-16(13,14)11-6-4-9(2)5-7-11/h3-7,10,12H,1,8H2,2H3/t10-/m0/s1
SMILES:C=C[C@@H](COS(=O)(=O)c1ccc(C)cc1)O
Synonyms:
  • (S)-3-Butene-1,2-Diol 1-Tosylate
  • (S)-2-Hydroxy-3-Buten-1-Yl P-Tosylate
  • (S)-2-Hydroxy-3-Buten-1-Yl Tosylate
  • (S)-2-Hydroxy-3-Butenyl-1-Tosylate
  • (S)-2-Hydroxy-3-Butenyl Tosylate
  • (S)-3-Butene-1,2-diol-1-(p-toluenesulfonate)
  • (S)-2-Hydroxy-3-Buten-1-Yl P-Tosylate, 99%(Gc)
  • (2S)-2-hydroxybut-3-en-1-yl 4-methylbenzenesulfonate
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