CymitQuimica logo

CAS 138249-07-7

:

(R)-1-TOSYLOXY-3-BUTEN-2-OL

Description:
(R)-1-Tosyloxy-3-buten-2-ol is an organic compound characterized by the presence of a tosylate functional group, which enhances its reactivity in various chemical reactions, particularly in nucleophilic substitutions. This compound features a butenol structure, indicating the presence of a double bond and an alcohol group, which contributes to its potential as a chiral building block in organic synthesis. The (R) configuration denotes the specific stereochemistry at the chiral center, which is crucial for its application in asymmetric synthesis. The tosylate group is known for its ability to act as a good leaving group, facilitating reactions such as elimination and substitution. Additionally, the compound's solubility and reactivity can be influenced by the presence of the tosyl group, making it a valuable intermediate in the synthesis of more complex molecules. Its applications may extend to pharmaceuticals and agrochemicals, where chirality plays a significant role in biological activity. Overall, (R)-1-tosyloxy-3-buten-2-ol is a versatile compound in synthetic organic chemistry.
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-/m1/s1
SMILES:C=C[C@H](COS(=O)(=O)c1ccc(C)cc1)O
Synonyms:
  • (R)-3-Butene-1,2-Diol 1-Tosylate
  • (R)-2-Hydroxy-3-Buten-1-Yl P-Tosylate
  • (R)-2-Hydroxy-3-Buten-1-Yl Tosylate
  • (R)-2-Hydroxy-3-Butenyl-1-Tosylate
  • (R)-2-Hydroxy-3-Butenyl Tosylate
  • Rarechem Ak Hz 0031
  • (R)-3-Butene-1,2-diol-1-(p-toluenesulfonate)
  • (2R)-2-hydroxybut-3-en-1-yl 4-methylbenzenesulfonate
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
Found 2 products.