CAS 189307-64-0
:(1S,3R,5R,6S,8S,10R,11S,13R,15R,16S,18R,20R,21S,23R,25R,26S,28R,30R,31S,33R,35R,36S,38R,40R,41R,42R,43R,44R,45R,46R,47R,48R,49R,50R,51R,52R,53R,54R,55S,56S)-55-amino-5,10,15,20,25,30,35,40-octakis(hidroximetil)-2,4,7,9,12,14,17,19,22,24,27,29,32,34,37,39
Descripción:
La sustancia química con el nombre "(1S,3R,5R,6S,8S,10R,11S,13R,15R,16S,18R,20R,21S,23R,25R,26S,28R,30R,31S,33R,35R,36S,38R,40R,41R,42R,43R,44R,45R,46R,47R,48R,49R,50R,51R,52R,53R,54R,55S,56S)-55-amino-5,10,15,20,25,30,35,40-octakis(hidroximetil)-2,4,7,9,12,14,17,19,22,24,27,29,32,34,37,39" y el número CAS "189307-64-0" es una molécula orgánica compleja caracterizada por una estereoquímica altamente específica, indicada por su extenso uso de estereocentros. Este compuesto presenta múltiples grupos hidroximetilo, lo que sugiere un alto grado de funcionalización, potencialmente mejorando su solubilidad y reactividad. La presencia de un grupo amino indica potencial para actividad biológica, posiblemente sirviendo como un ligando o un precursor en vías sintéticas. La intrincada disposición de centros quirales implica que esta sustancia puede exhibir propiedades ópticas únicas y podría ser de interés en campos como la química medicinal o la ciencia de materiales. Su complejidad estructural también puede sugerir desafíos en la síntesis y purificación, convirtiéndola en un tema de interés para investigadores que se centran en la síntesis asimétrica y técnicas de resolución quiral.
Fórmula:C48H81NO39·H2O
InChI:InChI=1/C48H81NO39/c49-17-18(58)41-73-9(1-50)33(17)81-42-26(66)19(59)35(11(3-52)74-42)83-44-28(68)21(61)37(13(5-54)76-44)85-46-30(70)23(63)39(15(7-56)78-46)87-48-32(72)25(65)40(16(8-57)80-48)88-47-31(71)24(64)38(14(6-55)79-47)86-45-29(69)22(62)36(12(4-53)77-45)84-43-27(67)20(60)34(82-41)10(2-51)75-43/h9-48,50-72H,1-8,49H2/t9-,10-,11-,12-,13-,14-,15-,16-,17+,18+,19-,20-,21-,22-,23-,24-,25-,26-,27-,28-,29-,30-,31-,32-,33-,34-,35-,36-,37-,38-,39-,40-,41-,42-,43-,44-,45-,46-,47-,48-/m1/s1
Sinónimos:- (1S,3R,5R,6S,8S,10R,11S,13R,15R,16S,18R,20R,21S,23R,25R,26S,28R,30R,31S,33R,35R,36S,38R,40R,41R,42R,43R,44R,45R,46R,47R,48R,49R,50R,51R,52R,53R,54R,55S,56S)-55-Amino-5,10,15,20,25,30,35,40-octakis(hydroxymethyl)-2,4,7,9,12,14,17,19,22,24,27,29,32,34,37,39-hexadecaoxanonacyclo[36.2.2.23,6
- S
- 3A-Amino-3A-deoxy-(2AS,3AS)-gamma-cyclodextrin Hydrate
- 3A-Amino-3A-deoxy-(2A
- )-&gamma
- 3A-Amino-3A-deoxy-(2AS,3AS)-gamma-cyclodextrin
- ,3A
- γ-Cyclodextrin, 3A-amino-3A-deoxy-, (2AS,3AS)-
- 3A-AMino-3A-deoxy-(2AS,3AS)-gaMMa-cyclodextrin 
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Encontrado 3 productos.
3A-Amino-3a-deoxy-(2as,3as)-γ-cyclodextrin hydrate
CAS:Fórmula:C48H81NO39Forma y color:SolidPeso molecular:1296.14003A-Amino-3a-deoxy-(2as,3as)-γ-cyclodextrin Hydrate
CAS:Producto controlado<p>Applications 3A-Amino-3a-deoxy-(2as,3as)-gamma-cyclodextrin hydrate is a useful research compound, a cyclodextrin derivative.<br>References Oka, Y., et al.: Anal. Sci., 28, 973 (2012); Teranishi, K., et al.: Luminescence, 14, 303 (1999)<br></p>Fórmula:C48H81NO39Forma y color:NeatPeso molecular:1296.146-Monodeoxy-6-monoamino-gamma-cyclodextrin,
CAS:<p>This gamma-cyclodextrin (γ-CD) derivative is a modified cyclic oligosaccharide composed of eight glucose units, featuring a larger cavity size than α- and β-cyclodextrins. This structural characteristic allows γ-CDs to form inclusion complexes with a wider range of guest molecules, making it particularly versatile in various industries. In the food sector, it is used as a carrier and stabilizer for flavors, fat-soluble vitamins, and polyunsaturated fatty acids, protecting volatile compounds from evaporation. In pharmaceuticals, it enhances the solubility and bioavailability of poorly water-soluble drugs and, thanks to its larger ring size, allows for the encapsulation of larger molecules or even entire drug molecules. γ-CDs and derivatives are also used for environmental remediation and, in analytical chemistry, for the extraction and concentration of target substances.</p>Fórmula:C48H81NO39Pureza:Min. 95%Peso molecular:1,296.14 g/mol



