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CAS Number: 871038-72-1
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CAS Number
871038-72-1
PubChem CID
23668479
Molecular Formula
C20H20FKN6O5
Molecular Weight
482.5 g/mol
Exact Mass
482.111627
InChIKey
IFUKBHBISRAZTF-UHFFFAOYSA-M
IUPAC Name
potassium 4-[(4-fluorophenyl)methylcarbamoyl]-1-methyl-2-[2-[(5-methyl-1,3,4-oxadiazole-2-carbonyl)amino]propan-2-yl]-6-oxopyrimidin-5-olate
SMILES String
Cc1nnc(C(=O)NC(C)(C)c2nc(C(=O)NCc3ccc(F)cc3)c([O-])c(=O)n2C)o1.[K+]
No physical property values available.
Properties are provided as catalog reference data and may be confirmed through supplier documentation when required.
Structural features
Raltegravir Potassium (CAS 871038-72-1) is listed in the Pharmaceutical Intermediates portfolio, with molecular formula C20H20FKN6O5 and molecular weight 482. 50 g/mol.
Sourcing context
Catalog reference for RFQ preparation, supplier confirmation, and research chemical sourcing review.
Research use context
Intended for research-stage medicinal chemistry and intermediate synthesis workflows; structure-derived tags include nitrogen-containing heterocycle.
Documentation needs
COA/SDS status, availability, lead time, pack size, and shipment documentation can be confirmed during quotation.
ChEMBL reports experimental activity evidence for: Human immunodeficiency virus type 1 integrase (Human immunodeficiency virus 1) — 3 assays. These records describe research assays and do not establish therapeutic efficacy or clinical use.
Human immunodeficiency virus type 1 integrase
Human immunodeficiency virus 1 · SINGLE PROTEIN · 3 qualifying assays · 3 documents · best pChEMBL 8.48
Experimental evidence source: ChEMBL
Safety and handling reference content is available through documentation requests.
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Preliminary Safety Reference
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Safety Reference / SDS RequestCatalog navigation
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Raltegravir Potassium is identified by CAS 871038-72-1, with molecular formula C20H20FKN6O5, molecular weight 482.5, InChIKey IFUKBHBISRAZTF-UHFFFAOYSA-M.
ChEMBL contains qualifying experimental assay evidence associated with Human immunodeficiency virus type 1 integrase. These records do not establish therapeutic efficacy or clinical use.
Yes. Submit an RFQ and specify COA requirements. Lot-specific COA depends on supplier confirmation.
Yes. Supplier SDS can be requested through the RFQ workflow before handling, storage, shipment, or procurement decisions.
Availability, pack size, lead time, and pricing are confirmed through RFQ.
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