CAS 70987-78-9
:(S)-Glicidil tosilo
Fórmula: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
Clave InChI:InChIKey=NOQXXYIGRPAZJC-VIFPVBQESA-N
SMILES:S(OC[C@@H]1CO1)(=O)(=O)C2=CC=C(C)C=C2
Sinónimos:- (+)-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
- 2-Oxiranemethanol, 2-(4-methylbenzenesulfonate), (2S)-
- Oxiranemethanol, 4-methylbenzenesulfonate, (2S)-
- Oxiranemethanol, 4-methylbenzenesulfonate, (S)-
- S-Glycidyl Tosylate
- Toluene-4-sulfonic acid (S)-oxiranylmethyl ester
- [(2S)-Oxiran-2-yl]methyl 4-methylbenzene-1-sulfonate
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Se han encontrado 9 productos.
(2S)-(+)-Glycidyl p-Toluenesulfonate
CAS:Fórmula:C10H12O4SPureza:>98.0%(GC)Forma y color:White to Almost white powder to crystalPeso molecular:228.26(2S)-Oxiran-2-ylmethyl 4-methylbenzenesulphonate
CAS:(2S)-Oxiran-2-ylmethyl 4-methylbenzenesulphonateFórmula:C10H12O4SPureza:98%Forma y color:SolidPeso molecular:228.26488(s)-(+)-oxirane-2-methanol p-toluenesulfonate
CAS:(s)-(+)-oxirane-2-methanol p-toluenesulfonateFórmula:C10H12O4SPureza:98%Peso molecular:228.26(2S)-(+)-Glycidyl Tosylate
CAS:Producto controladoApplications 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),Fórmula:C10H12O4SForma y color:NeatPeso molecular:228.26(2S)-Oxiran-2-ylmethyl 4-methylbenzenesulfonate
CAS:Fórmula:C10H12O4SPureza:98%Forma y color:White to Yellow SolidPeso molecular: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 isolatedFórmula:C10H12O4SPureza:Min. 95%Forma y color:PowderPeso molecular:228.27 g/mol








