1-Cyano-N-(4-fluorophenyl)pyrrolo[2,1-a]isoquinoline-3-carboxamide CAS 618444-02-3

Purity 97%+In StockPharmaceutical Standards
CAS No.618444-02-3
Molecular FormulaC20H12FN3O
Molecular Weight329.33 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

1-Cyano-N-(4-fluorophenyl)pyrrolo[2,1-a]isoquinoline-3-carboxamide CAS 618444-02-3 chemical structure

Description

CATO supplies 1-Cyano-N-(4-fluorophenyl)pyrrolo[2,1-a]isoquinoline-3-carboxamide (CAS 618444-02-3), a certified reference material (molecular formula C20H12FN3O, MW 329.33 g/mol) for analytical method development and quality control.

1-Cyano-N-(4-fluorophenyl)pyrrolo[2,1-a]isoquinoline-3-carboxamide (C20H12FN3O) contains a steroid core, an amide group, a hydroxyl group, an ether linkage, fluorine substitution. Halogen substitution raises its density and boiling point, its high carbon-to-hydrogen ratio confers good lipid solubility; these physicochemical properties determine the optimal preparation and storage of its standard solutions. The high carbon-to-hydrogen ratio imparts good lipophilicity, allowing liquid-liquid extraction with non-polar solvents such as n-hexane or ethyl acetate.

Recommended for analytical method development and validation; each product is supplied with a full Certificate of Analysis (COA) ensuring ISO 17034 metrological traceability.

CATO manufactures 1-Cyano-N-(4-fluorophenyl)pyrrolo[2,1-a]isoquinoline-3-carboxamide under ISO 17034:2016 accreditation with dual CNAS and ANAB accreditation. Each batch is characterized by orthogonal methods and supplied with a full Certificate of Analysis (COA), ensuring metrological traceability.

Physical & Chemical Properties

Molecular FormulaC20H12FN3O
Molecular Weight329.33 g/mol
AppearancePale yellow to yellow crystalline powder. (slight halide-like odor)
Purity97%+
StorageStore at 2-8°C, protect from light
Solubility (reference)Soluble in DMSO, DMF, methanol
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)16.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1985
Halogen ContentF-containing
Nitrogen Atoms3

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