Grundinformationen
- Standard-SMILES
Cc1ccc(S(=O)(=O)OCC2CO2)cc1- InChIKey
NOQXXYIGRPAZJC-UHFFFAOYSA-N- Summenformel
- C10H12O4S
- Durchschnittliche Molmasse
- 228,27 g/mol
- Monoisotopische Masse
- 228,04563003
Namen und Bezeichner
- Bevorzugter Name
- Glycidyl tosylate
- IUPAC
- oxiran-2-ylmethyl 4-methylbenzenesulfonate
- Englischer Name
- Glycidyl 4-toluenesulfonate
- Summenformel
- C10H12O4S
- Molmasse
- 228.26
Namen und Synonyme
6746-81-2Glycidyl tosylateQT428577JZRefChem:922337Oxiran-2-ylmethyl 4-methylbenzenesulfonateGlycidyl 4-toluenesulfonatetoluene-4-sulfonic acid oxiranylmethyl ester(oxiran-2-yl)methyl 4-methylbenzene-1-sulfonateMFCD00066850SCHEMBL439063(S)-2,3-EPOXY-1-PROPYL P-TOLUENESULFONATENSC-143322
Weitere Namen anzeigen
Glyceryl 4-toluenesulfonate2,3-Epoxypropyl p-toluenesulfonate2-Oxiranemethanol,2-(4-methylbenzenesulfonate)5-Methyl-2-(oxiran-2-ylMethyl)benzene-1-sulfonate
Oxiranemethanol, 4-methylbenzenesulfonateCS-01875992,3-EPOXY-1-PROPYL P-TOLUENESULFONATE(2R)-Glycidyl tosylate(R)-(-)-Glycidyl tosylate2-Oxiranylmethyl 4-methylbenzenesulfonateNSC636971SY017230
Datenbank-Bezeichner
- CAS
6746-81-2- PubChem CID
- 160868
- DTXSID
DTXSID40867977- UNII
- QT428577JZ
- Nikkaji
- J313.376A
Eigenschaften
Berechnete Struktureigenschaften
- XLogP
- 1,1
- Polarare Oberfläche (TPSA)
- 64,3 Ų
- H-Brücken-Donoren
- 0
- H-Brücken-Akzeptoren
- 4
- Frei drehbare Bindungen
- 4
- Schwere Atome
- 15
- Formalladung
- 0
- Komplexität
- 298
Physikochemische Eigenschaften
- Siedepunkt
- 95 · 95-100 °C(Press: 0.01 Torr)
- Dichte
- 1.31 · 1.310±0.06 g/cm3(Predicted)
- storage temp.
- -20 °C · -20°C Freezer, Under inert atmosphere
- Löslichkeit
- Chloroform (Sparingly), Methanol (Slightly)
- Aggregatzustand
- Solid
- Farbe
- White to Off-White
- InChI
- InChI=1S/C10H12O4S/c1-8-2-4-10(5-3-8)15(11,12)14-7-9-6-13-9/h2-5,9H,6-7H2,1H3
- InChIKey
- NOQXXYIGRPAZJC-UHFFFAOYSA-N
- SMILES
- C1(=CC=C(C)C=C1)S(=O)(=O)OCC1OC1
Chemie und Industrie
Anwendungen
VerwendenGlycidyl 4-Toluenesulfonate is used in the development and validation of a chiral HPLC method for rapid screening of allylic alcohol asymmetric epoxidation processes. Glycidyl 4-Toluenesulfonate is a reagent for organic displacement, additional and ring-opening reactions.
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