CAS 136310-64-0
:(1α,2β,4β,5α,7β)-9-Metil-3-oxa-9-azatriciclo[3.3.1.02,4]non-7-il α-hidroxi-α-2-tienil-2-tiofenoacetato
Descripción:
La sustancia química conocida como "(1α,2β,4β,5α,7β)-9-Metil-3-oxa-9-azatriciclo[3.3.1.02,4]non-7-il α-hidroxi-α-2-tienil-2-tiofenoacetato" con número CAS 136310-64-0 es un compuesto orgánico complejo caracterizado por su estructura bicyclic única y la presencia de múltiples grupos funcionales. Este compuesto presenta un marco tricíclico que incluye tanto átomos heteroatómicos de nitrógeno como de oxígeno, lo que contribuye a su potencial actividad biológica. La presencia de grupos tiénilo y tiofeno sugiere que puede exhibir propiedades electrónicas y reactividad interesantes, que podrían ser relevantes en la química medicinal. El grupo α-hidroxilo indica potencial para enlaces de hidrógeno y reactividad en varios entornos químicos. En general, la complejidad estructural y la diversidad funcional de este compuesto pueden proporcionar vías para la investigación en farmacología y ciencia de materiales, aunque las actividades biológicas específicas y las aplicaciones requerirían una investigación adicional a través de estudios empíricos.
Fórmula:C18H19NO4S2
InChI:InChI=1/C18H19NO4S2/c1-19-11-8-10(9-12(19)16-15(11)23-16)22-17(20)18(21,13-4-2-6-24-13)14-5-3-7-25-14/h2-7,10-12,15-16,21H,8-9H2,1H3/t10-,11-,12+,15-,16+
Clave InChI:InChIKey=VPJFFOQGKSJBAY-FDAWXEHDNA-N
SMILES:CN1[C@@]2([C@]3([C@](O3)([C@]1(C[C@@H](OC(C(O)(C4=CC=CS4)C5=CC=CS5)=O)C2)[H])[H])[H])[H]
Sinónimos:- (1α,2β,4β,5α,7β)-7-[(Hydroxydi(2-thienyl)acetyl)oxy]-9-methyl-3-oxa-9-azatricyclo[3.3.1.0]nonane
- (1α,2β,4β,5α,7β)-9-Methyl-3-oxa-9-azatricyclo[3.3.1.0<sup>2,4</sup>]non-7-yl α-hydroxy-α-2-thienyl-2-thiopheneacetate
- 2-Thiopheneacetic acid, α-hydroxy-α-2-thienyl-, (1α,2β,4β,5α,7β)-9-methyl-3-oxa-9-azatricyclo[3.3.1.0<sup>2,4</sup>]non-7-yl ester
- 2-Thiopheneacetic acid, α-hydroxy-α-2-thienyl-, 9-methyl-3-oxa-9-azatricyclo[3.3.1.0<sup>2,4</sup>]non-7-yl ester, (1α,2β,4β,5α,7β)-
- 9-Methyl-3-Oxa-9-Azatricyclo[3.3.1.02,4]Non-7-Yl Hydroxy(Dithiophen-2-Yl)Acetate
- Di(2-thienyl)glycolic acid scopine ester
- Dithienylglycolic acid scopine ester
- N-Demethyl tiotropium
- Scopine di(2-thienylglycolate)
- Scopine hydroxydi(2-thienyl)acetate
- Scopine-2,2-Dithienyl Glycolate
- 2-Thiopheneacetic acid, α-hydroxy-α-2-thienyl-, 9-methyl-3-oxa-9-azatricyclo[3.3.1.02,4]non-7-yl ester, (1α,2β,4β,5α,7β)-
- 2-Thiopheneacetic acid, α-hydroxy-α-2-thienyl-, (1α,2β,4β,5α,7β)-9-methyl-3-oxa-9-azatricyclo[3.3.1.02,4]non-7-yl ester
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Encontrado 10 productos.
Scopine di(2-thienylglycolate) (2-Thiopheneacetic acid, α-hydroxy-α-2-thienyl-, (1α,2β,4β,5α,7β)-9-methyl-3-oxa-9-azatricyclo[3.3.1.0 2,4]non-7-yl ester)
CAS:Nucleic acids and their salts, whether or not chemically defined; other heterocyclic compounds, nesoiFórmula:C18H19NO4S2Forma y color:White Off-White PowderPeso molecular:377.075552-Thiopheneacetic acid, α-hydroxy-α-2-thienyl-, (1α,2β,4β,5α,7β)-9-methyl-3-oxa-9-azatricyclo[3.3.1.02,4]non-7-yl ester
CAS:Fórmula:C18H19NO4S2Pureza:96%Forma y color:SolidPeso molecular:377.4778Tiotropium Bromide Impurity 24
CAS:Fórmula:C18H19NO4S2Forma y color:White To Off-White SolidPeso molecular:377.47rel-(1R,2R,4S,5S,7s)-9-Methyl-3-oxa-9-azatricyclo[3.3.1.02,4]nonan-7-yl 2-hydroxy-2,2-di(thiophen-2-yl)acetate
CAS:rel-(1R,2R,4S,5S,7s)-9-Methyl-3-oxa-9-azatricyclo[3.3.1.02,4]nonan-7-yl 2-hydroxy-2,2-di(thiophen-2-yl)acetatePureza:96%Peso molecular:377.49g/molTiotropium EP Impurity B
CAS:Producto controladoFórmula:C18H19NO4S2Forma y color:NeatPeso molecular:377.48Scopine Di(2-thienylglycolate)
CAS:<p>Impurity Tiotropium EP Impurity B<br>Applications Scopine Di(2-thienylglycolate) (Tiotropium EP Impurity B) is a precursor to Tiotropium Bromide.<br>References Buchwald, P., et al.: Pharmazie., 55, S210 (2000),<br></p>Fórmula:C18H19NO4S2Forma y color:NeatPeso molecular:377.48Scopine di(2-thienyl)glycolate
CAS:Fórmula:C18H19NO4S2Pureza:96%Forma y color:SolidPeso molecular:377.47Scopine-2,2-dithienyl glycolate
CAS:<p>Scopine-2,2-dithienyl glycolate is a catalyst that belongs to the class of dithienyl glycolates. Scopine-2,2-dithienyl glycolate is used in the pharmaceutical industry as an average catalyst for reactions and can be used to recover dimethylbenzene. The method of detection for scopine-2,2-dithienyl glycolate is based on its ability to absorb light at a wavelength of 360 nm. The reaction solution must be monitored carefully during the synthetic process because it has been shown that it can react with water or air and form hydrogen sulfide gas. If this happens, the reaction solution will become cloudy or turbid. This product is a white crystalline solid that appears as tiny needles and has a melting point of 173 degrees Celsius (340 degrees Fahrenheit).</p>Fórmula:C18H19NO4S2Pureza:Min. 95%Peso molecular:377.48 g/mol










