4-(3-(Trifluoromethyl)phenyl)-1H-pyrrolo[2,3-b]pyridine CAS 916173-13-2

Purity 97%+In StockPharmaceutical Standards
CAS No.916173-13-2
Molecular FormulaC14H9F3N2
Molecular Weight262.23 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

4-(3-(Trifluoromethyl)phenyl)-1H-pyrrolo[2,3-b]pyridine CAS 916173-13-2 chemical structure

Description

Compared with other compounds in its class, the molecular weight of 262.23 g/mol gives 4-(3-(Trifluoromethyl)phenyl)-1H-pyrrolo[2,3-b]pyridine distinctive chromatographic separation conditions and mass-spectrometry parameter settings.

4-(3-(Trifluoromethyl)phenyl)-1H-pyrrolo[2,3-b]pyridine (CAS 916173-13-2) is a high-purity analytical reference standard with the molecular formula C14H9F3N2 and a molecular weight of 262.23 g/mol.

4-(3-(Trifluoromethyl)phenyl)-1H-pyrrolo[2,3-b]pyridine (C14H9F3N2) contains a nitrogen-containing heterocyclic scaffold, a nitrile group, 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. Nitrogen-containing functional groups confer excellent ionization efficiency in positive-ion electrospray (ESI) mode, making the compound well suited to LC-MS/MS analysis.

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

The assigned purity is verified by mass-balance and quantitative NMR (qNMR) approaches, with the expanded uncertainty reported at a 95% confidence level (k=2). Batch homogeneity and stability are independently assessed for every lot.

Physical & Chemical Properties

Molecular FormulaC14H9F3N2
Molecular Weight262.23 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light, keep tightly closed to prevent evaporation
Solubility (reference)Soluble in DMSO, DMF, methanol
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)10.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1987
Halogen ContentF-containing
Nitrogen Atoms2

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