CAS 70987-78-9: (S)-Glycidyl tosylate
Formula:C10H12O4S
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/t9-/m0/s1
InChI key:InChIKey=NOQXXYIGRPAZJC-VIFPVBQESA-N
SMILES:S(OC[C@@H]1CO1)(=O)(=O)C2=CC=C(C)C=C2
Synonyms:- (+)-Glycidyl tosylate
- (2S)-(+)-Glycidyl Tosylate
- (2S)-Glycidyl toslyate
- (2S)-Oxiranemethanol 4-methylbenzenesulfonate
- (S)-(+)-Glycidyl 4-methylbenzenesulfonate
- (S)-(2,3-Epoxypropan-1-yl) 4-methylbenzenesulfonate
- (S)-Glycidol tosylate
- (S)-Glycidyl p-toluenesulfonate
- (S)-Oxiranylmethyl toluene-4-sulfonate
- (S)-Toluene-4-sulfonic acid oxiranylmethyl ester
- 2(S)-Glycidyl tosylate
- See more synonyms
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Found 10 products.
(2S)-(+)-Glycidyl Tosylate
CAS:Controlled ProductApplications Protected Glycidol, used as an intermediate in the preparation of neurochemicals. References Wang, J., et al.: J. Med. Chem., 48, 6271 (2005), Qian, L., et al.: ChemMedChem, 1, 376 (2006), Li, Y., et al.: Bioorg. Med. Chem. Lett., 19, 5037 (2009),Formula:C10H12O4SColor and Shape:Off-WhiteMolecular weight:228.26(2S)-(+)-Glycidyl tosylate
CAS:Formula:C10H12O4SPurity:97%Color and Shape:SolidMolecular weight:228.2649(2S)-Oxiran-2-ylmethyl 4-methylbenzenesulphonate
CAS:(2S)-Oxiran-2-ylmethyl 4-methylbenzenesulphonatePurity:98+%Molecular weight:228.26g/mol(2S)-Oxiran-2-ylmethyl 4-methylbenzenesulfonate
CAS:Purity:99.0%Color and Shape:Solid, White to Yellow SolidMolecular weight:228.25999450683594(S)-Glycidyl tosylate
CAS:Controlled ProductFormula:C10H12O4SColor and Shape:NeatMolecular weight:228.26(2S)-(+)-Glycidyl p-Toluenesulfonate
CAS:Formula:C10H12O4SPurity:>98.0%(GC)Color and Shape:White to Almost white powder to crystalMolecular weight:228.26S-(+)-Glycidyl tosylate
CAS:S-(+)-Glycidyl tosylate is a cross-linking agent that can be used in the preparation of polymers. It has been shown to react with epoxides and hydroxyl groups, but not with hydroxy groups. S-(+)-Glycidyl tosylate is also considered a nucleophilic reagent that reacts with nucleophiles such as amines, alcohols, and thiols. This product is an enantiomer of racemic glycidyl tosylate, which is a reaction intermediate for the synthesis of epoxy resins. The use of this product may lead to the production of hard and brittle materials due to its ability to form strong covalent bonds. S-(+)-Glycidyl tosylate was first synthesized by reacting ethylene oxide with chloroacetic acid followed by hydrolysis of the resulting chloroacetaldehyde ester using an acid catalyst. The isolatedFormula:C10H12O4SPurity:Min. 95%Color and Shape:PowderMolecular weight:228.27 g/mol
