![1H-as-Indaceno[3,2-d]oxacyclododecin-7,15-dione, 2-[(6-deoxy-3-O-ethyl-2,4-di-O-methyl-α-L-mannopy…](/_next/image/?url=https%3A%2Fstatic.cymitquimica.com%2Fcas-image%2Fthumb-webp%2F397458-1h-as-indaceno-32-d-oxacyclododecin-715-dione-2-6-deoxy-3-o-ethyl-24-di-o-methyl-a-l-mannopyranosyl-oxy-13-2r-5s-6r-5-dimethylamino-tetrahydro-6-methyl-2h-pyran-2-yl-oxy-9-ethyl-233a-455a-5b-69101112131416a-16b-hexadecahydro-14-methyl-2r-3ar-5a.webp&w=3840&q=75)
CAS 187166-40-1: 1H-as-Indaceno[3,2-d]oxaciclododecina-7,15-diona, 2-[(6-desoxi-3-O-etil-2,4-di-O-metil-α-L-manopiranosil)oxi]-13-[[(2R,5S,6R)-5-(dimetilamino)tetrahidro-6-metil-2H-piran-2-il]oxi]-9-etil-2,3,3a,4,5,5a,5b,6,9,10,11,12,13,14,16a,16b-hexadecahidro-14-metil-, (2R,3aR,5aR,5bS,9S,13S,14R,16aS,16bR)-
Descripción:
La sustancia química conocida como 1H-as-Indaceno[3,2-d]oxaciclododecina-7,15-diona, con el número CAS 187166-40-1, es un compuesto orgánico complejo caracterizado por su intrincada estructura molecular, que incluye múltiples grupos funcionales y estereocentros. Este compuesto presenta una estructura central bicíclica, indicativa de su marco indaceno, e incorpora un moiety oxaciclododecina, sugiriendo aplicaciones potenciales en química medicinal debido a su disposición única de átomos de carbono y oxígeno. La presencia de un moiety de azúcar, específicamente un grupo α-L-mannopiranosilo modificado, indica que este compuesto puede exhibir actividad biológica, posiblemente interactuando con sistemas biológicos a través de la glicosilación. Además, el grupo dimetilamino y varios sustituyentes alquilo contribuyen a su lipofilia y propiedades farmacológicas potenciales. La estereoquímica del compuesto, denotada por las configuraciones R y S específicas, es crucial para su actividad biológica, ya que puede influir en cómo la molécula interactúa con los objetivos biológicos. En general, este compuesto representa un fascinante ejemplo de la intersección entre la química orgánica y la farmacología, justificando una investigación más profunda sobre sus propiedades y usos potenciales.
Fórmula:C42H69NO10
InChI:InChI=1S/C42H69NO10/c1-10-27-13-12-14-35(53-37-18-17-34(43(6)7)24(4)49-37)23(3)38(45)33-21-31-29(32(33)22-36(44)51-27)16-15-26-19-28(20-30(26)31)52-42-41(47-9)40(48-11-2)39(46-8)25(5)50-42/h21,23-32,34-35,37,39-42H,10-20,22H2,1-9H3/t23-,24-,25+,26-,27+,28-,29-,30-,31-,32+,34+,35+,37+,39+,40-,41-,42+/m1/s1
Clave InChI:InChIKey=GOENIMGKWNZVDA-RWGFPKGXSA-N
SMILES:O([C@H]1C[C@]2([C@]3([C@]([C@]4(C(=C3)C(=O)[C@H](C)[C@@H](O[C@@H]5O[C@H](C)[C@@H](N(C)C)CC5)CCC[C@H](CC)OC(=O)C4)[H])(CC[C@@]2(C1)[H])[H])[H])[H])[C@H]6[C@H](OC)[C@H](OCC)[C@@H](OC)[C@H](C)O6
Sinónimos:- (2R,3aR,5aR,5bS,9S,13S,14R,16aS,16bR)-2-[(6-Deoxy-3-O-ethyl-2,4-di-O-methyl-α-<span class="text-smallcaps">L</span>-mannopyranosyl)oxy]-13-[[(2R,5S,6R)-5-(dimethylamino)tetrahydro-6-methyl-2H-pyran-2-yl]oxy]-9-ethyl-2,3,3a,4,5,5a,5b,6,9,10,11,12,13,14,16a,16b-hexadecahydro-14-methyl-1H-as-indaceno[3,2-d]oxacyclododecin-7,15-dione
- 187166-15-0
- 187166-40-1
- 1H-as-Indaceno[3,2-d]oxacyclododecin-7,15-dione, 2-[(6-deoxy-3-O-ethyl-2,4-di-O-methyl-α-<span class="text-smallcaps">L</span>-mannopyranosyl)oxy]-13-[[(2R,5S,6R)-5-(dimethylamino)tetrahydro-6-methyl-2H-pyran-2-yl]oxy]-9-ethyl-2,3,3a,4,5,5a,5b,6,9,10,11,12,13,14,16a,16b-hexadecahydro-14-methyl-, (2R,3aR,5aR,5bS,9S,13S,14R,16aS,16bR)-
- 1H-as-Indaceno[3,2-d]oxacyclododecin-7,15-dione, 2-[(6-deoxy-3-O-ethyl-2,4-di-O-methyl-α-<span class="text-smallcaps">L</span>-mannopyranosyl)oxy]-13-[[(2R,5S,6R)-5-(dimethylamino)tetrahydro-6-methyl-2H-pyran-2-yl]oxy]-9-ethyl-2,3,3a,4,5,5a,5b,6,9,10,11,12,13,14,16a,16b-hexadecahydro-14-methyl-, [2R-(2R*,3aR*,5aR*,5bS*,9S*,13S*,14R*,16aS*,16bR*)]-
- De 175J
- Spinetoram J
- Xde 175J
- 1H-as-Indaceno[3,2-d]oxacyclododecin-7,15-dione, 2-[(6-deoxy-3-O-ethyl-2,4-di-O-methyl-α-L-mannopyranosyl)oxy]-13-[[(2R,5S,6R)-5-(dimethylamino)tetrahydro-6-methyl-2H-pyran-2-yl]oxy]-9-ethyl-2,3,3a,4,5,5a,5b,6,9,10,11,12,13,14,16a,16b-hexadecahydro-14-methyl-, (2R,3aR,5aR,5bS,9S,13S,14R,16aS,16bR)-
- 1H-as-Indaceno[3,2-d]oxacyclododecin-7,15-dione, 2-[(6-deoxy-3-O-ethyl-2,4-di-O-methyl-α-L-mannopyranosyl)oxy]-13-[[(2R,5S,6R)-5-(dimethylamino)tetrahydro-6-methyl-2H-pyran-2-yl]oxy]-9-ethyl-2,3,3a,4,5,5a,5b,6,9,10,11,12,13,14,16a,16b-hexadecahydro-14-methyl-, [2R-(2R*,3aR*,5aR*,5bS*,9S*,13S*,14R*,16aS*,16bR*)]-
- (2R,3aR,5aR,5bS,9S,13S,14R,16aS,16bR)-2-[(6-Deoxy-3-O-ethyl-2,4-di-O-methyl-α-L-mannopyranosyl)oxy]-13-[[(2R,5S,6R)-5-(dimethylamino)tetrahydro-6-methyl-2H-pyran-2-yl]oxy]-9-ethyl-2,3,3a,4,5,5a,5b,6,9,10,11,12,13,14,16a,16b-hexadecahydro-14-methyl-1H-as-indaceno[3,2-d]oxacyclododecin-7,15-dione
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Encontrado 14 productos.
Pesticide Mixture 205 100 µg/mL in Acetonitrile
CAS:- 103055-07-8
- 107534-96-3
- 1113-02-6
- 111988-49-9
- 112410-23-8
- 116714-46-6
- 121-75-5
- 129558-76-5
- 138261-41-3
- 141517-21-7
- 148-79-8
- 161050-58-4
- 16752-77-5
- 168316-95-8
- 175013-18-0
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- 2312-35-8
- 23135-22-0
- 24017-47-8
- 2597-03-7
- 41198-08-7
- 53112-28-0
- 57837-19-1
- 67747-09-5
- 950-37-8
Fórmula:C9H10ClN5O2Forma y color:MixturePeso molecular:255.66California Pesticide Class 2B Mixture 100 µg/mL in Acetonitrile
CAS:Producto controlado- 107534-96-3
- 121-75-5
- 138261-41-3
- 141517-21-7
- 143390-89-0
- 153719-23-4
- 16752-77-5
- 168316-95-8
- 187166-40-1
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- 283594-90-1
- 300-76-5
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- 732-11-6
- 78587-05-0
- 8003-34-7
- 82-68-8
- 88671-89-0
- 96489-71-3
Fórmula:C17H21ClN2O2SForma y color:MixturePeso molecular:352.88Nevada Pesticide Mixture Version 2 100 µg/mL in Acetonitrile
CAS:Producto controlado- 110488-70-5
- 126833-17-8
- 131341-86-1
- 138261-41-3
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- 149877-41-8
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- 153719-23-4
- 158062-67-0
- 1596-84-5
- 168316-95-8
- 187166-40-1
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- 51-03-6
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- 68359-37-5
- 71751-41-2
- 76738-62-0
- 8003-34-7
- 82657-04-3
- 82-68-8
- 88671-89-0
Fórmula:C48H72O14cC47H70O14cmixForma y color:MixturePeso molecular:1732.13California Pesticides Class 2B Mixture 1035 100 µg/mL in Acetonitrile, Second Source
CAS:Producto controlado- 107534-96-3
- 121-75-5
- 138261-41-3
- 141517-21-7
- 143390-89-0
- 153719-23-4
- 16752-77-5
- 168316-95-8
- 187166-40-1
- 203313-25-1
- 23031-36-9
- 23135-22-0
- 283594-90-1
- 300-76-5
- 51-03-6
- 52645-53-1
- 57837-19-1
- 60207-90-1
- 732-11-6
- 78587-05-0
- 8003-34-7
- 82-68-8
- 88671-89-0
- 96489-71-3
Fórmula:C17H21ClN2O2SForma y color:MixturePeso molecular:352.88Spinetoram-J
CAS:Producto controladoApplications Spinetoram belongs to spinosyn family of insecticides and shows potential of natural products research. References Kirst H. A.: J. Antibiot., 63, 101-111 (2010)Fórmula:C42H69NO10Forma y color:White To Light YellowPeso molecular:748 or 760California Pesticide Class 2B Mixture 100 µg/mL in Acetonitrile
CAS:Producto controlado- 107534-96-3
- 121-75-5
- 138261-41-3
- 141517-21-7
- 143390-89-0
- 153719-23-4
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- 168316-95-8
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- 23135-22-0
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- 300-76-5
- 51-03-6
- 52645-53-1
- 57837-19-1
- 60207-90-1
- 732-11-6
- 78587-05-0
- 8003-34-7
- 82-68-8
- 88671-89-0
- 96489-71-3
Fórmula:C17H21ClN2O2SForma y color:MixturePeso molecular:352.88Nevada Pesticide Mixture 62 100 µg/mL in Acetonitrile
CAS:Producto controlado- 110488-70-5
- 126833-17-8
- 131341-86-1
- 133-06-2
- 138261-41-3
- 141517-21-7
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- 168316-95-8
- 187166-40-1
- 203313-25-1
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- 52315-07-8
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- 68359-37-5
- 71751-41-2
- 8003-34-7
- 82657-04-3
- 82-68-8
- 88671-89-0
Fórmula:C48H72O14cC47H70O14cmixForma y color:MixturePeso molecular:1732.13California Supplemental Cannabis Pesticide Mixture 463 100 µg/mL in Acetonitrile
CAS:Producto controladoFórmula:C9H8Cl3NO2SForma y color:MixturePeso molecular:300.59Nevada Pesticide Mixture Version 2 100 µg/mL in Acetonitrile
CAS:Producto controlado- 110488-70-5
- 126833-17-8
- 131341-86-1
- 138261-41-3
- 141517-21-7
- 149877-41-8
- 153233-91-1
- 153719-23-4
- 158062-67-0
- 1596-84-5
- 168316-95-8
- 187166-40-1
- 203313-25-1
- 51-03-6
- 52315-07-8
- 57960-19-7
- 68359-37-5
- 71751-41-2
- 76738-62-0
- 8003-34-7
- 82657-04-3
- 82-68-8
- 88671-89-0
Fórmula:C48H72O14cC47H70O14cmixForma y color:MixturePeso molecular:1732.13Spinetoram J
CAS:Spinetoram is a novel insecticide that belongs to the class of chlorantraniliprole. Spinetoram is active against a broad spectrum of insects, including resistant strains. It has been shown to be effective in controlling lepidopteran larvae and adults, as well as some species of sawflies and beetles. Spinetoram J is an insecticide with high resistance and low toxicity. It has been shown to be safe for use on plants, animals, and humans. The spinetoram metabolite benzoate is not harmful to humans or mammals, but it may cause damage to plants or other organisms if used incorrectly. Spinetoram J has been shown to have both analytical and enzyme activity properties that are important for pest control.Fórmula:C42H69NO10Pureza:Min. 95%Forma y color:PowderPeso molecular:748 g/molRef: 3D-FS176183
Producto descatalogadoCanada Pesticide Mixture 1 50 µg/mL in Acetonitrile
CAS:Producto controlado- 107534-96-3
- 111812-58-9
- 111988-49-9
- 114-26-1
- 116-06-3
- 116714-46-6
- 121-75-5
- 13194-48-4
- 135410-20-7
- 138261-41-3
- 149877-41-8
- 153719-23-4
- 1563-66-2
- 158062-67-0
- 1596-84-5
- 165252-70-0
- 16752-77-5
- 168316-95-8
- 187166-40-1
- 188425-85-6
- 2032-65-7
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- 333-41-5
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- 51-03-6
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- 60-51-5
- 62-73-7
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- 76738-62-0
- 88671-89-0
Fórmula:C48H72O14cC47H70O14cmixForma y color:MixturePeso molecular:1732.13Spinetoram
CAS:Applications Spinetoram J is a component of Spinetoram (S683650), a compound that belongs to the spinosyn family of insecticides and shows potential of natural products research. Useful in cannabis testing kits as a component of pesticide mixes (P698240). Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package References Kirst H. A.: J. Antibiot., 63, 101-111 (2010)Fórmula:C42H69NO10Forma y color:NeatPeso molecular:748.00
