Search Results for " Upadacitinib "
Upadacitinib Impurity 15
| SZ CAT No: | SZ-U005017 |
| CAS No | NA |
| Mol.F. | C17H19F3N6O |
| Mol.Wt. | 380.4 |
| Inv. Status | Custom Synthesis |
Chemical Name: (3R,4S)-3-Ethyl-4-(3H-imidazo[1,2-a]pyrrolo[2,3-e]pyrazin-8-yl)-N-(2,2,2-trifluoroethyl)pyrrolidine-1-carboxamide compound with (3S,4R)-3-ethyl-4-(3H-imidazo[1,2-a]pyrrolo[2,3-e]pyrazin-8-yl)-N-(2,2,2-trifluoroethyl)pyrrolidine-1-carboxamide (1:1)
Shipping Temperature: Ambient
HSN Code: 38229010
Country of Origin: India
Smiles: CC[C@@H](CN(C(NCC(F)(F)F)=O)C1)[C@@H]1C2=CN=C3N2C(C=CN4)=C4N=C3.CC[C@H](CN(C(NCC(F)(F)F)=O)C5)[C@H]5C6=CN=C7N6C(C=CN8)=C8N=C7
Upadacitinib Impurity 15 is chemically (3R,4S)-3-Ethyl-4-(3H-imidazo[1,2-a]pyrrolo[2,3-e]pyrazin-8-yl)-N-(2,2,2-trifluoroethyl)pyrrolidine-1-carboxamide compound with (3S,4R)-3-ethyl-4-(3H-imidazo[1,2-a]pyrrolo[2,3-e]pyrazin-8-yl)-N-(2,2,2-trifluoroethyl)pyrrolidine-1-carboxamide (1:1). Upadacitinib Impurity 15 is supplied with detailed characterization data compliant with regulatory guideline. Upadacitinib Impurity 15 can be used for the analytical method development, method validation (AMV), Quality Controlled (QC) application for Abbreviated New Drug Application (ANDA) or during commercial production of Upadacitinib.
The product can be used as reference standards and further traceability against pharmacopeial standards (USP or EP) can be provided based on feasibility. SynZeal products are for analytical purpose only and not for human use.
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