Search Results for " Letermovir "
Letermovir Impurity 10
| SZ目录编号: | SZ-L052016 |
| CAS 号 | NA |
| 分子式 | C34H36F2N4O5 |
| 分子量 | 618.7 |
| 投资状态 | Custom Synthesis |
化学名称: Ethyl (E)-3-(2-((E)-N'-(2-((E)-3-ethoxy-3-oxoprop-1-en-1-yl)-6-fluorophenyl)-4-(3-methoxyphenyl)piperazine-1-carboximidamido)-3-fluorophenyl)acrylate
Shipping Temperature: Ambient
HSN Code: 38229010
Country of Origin: India
微笑: COC1=CC(N2CCN(/C(NC3=C(F)C=CC=C3/C=C/C(OCC)=O)=N/C4=C(F)C=CC=C4/C=C/C(OCC)=O)CC2)=CC=C1
Letermovir Impurity 10 is chemically Ethyl (E)-3-(2-((E)-N'-(2-((E)-3-ethoxy-3-oxoprop-1-en-1-yl)-6-fluorophenyl)-4-(3-methoxyphenyl)piperazine-1-carboximidamido)-3-fluorophenyl)acrylate. Letermovir Impurity 10 is supplied with detailed characterization data compliant with regulatory guideline. Letermovir Impurity 10 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 Letermovir.
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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