4-Fluoro-5-iodo-1H-pyrrolo[2,3-b]pyridine CAS 1638765-44-2

Purity 97%+In StockPharmaceutical Standards
CAS No.1638765-44-2
Molecular FormulaC7H4FIN2
Molecular Weight262.02 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

4-Fluoro-5-iodo-1H-pyrrolo[2,3-b]pyridine CAS 1638765-44-2 chemical structure

Description

CATO manufactures 4-Fluoro-5-iodo-1H-pyrrolo[2,3-b]pyridine 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.

4-Fluoro-5-iodo-1H-pyrrolo[2,3-b]pyridine (CAS 1638765-44-2) is a high-purity analytical reference standard with the molecular formula C7H4FIN2 and a molecular weight of 262.02 g/mol.

Owing to a nitrile group, fluorine/iodine substitution, an aromatic ring system, 4-Fluoro-5-iodo-1H-pyrrolo[2,3-b]pyridine is typically off-white to pale yellow crystalline powder. Its solid-state physicochemical attributes — including a molecular weight of 262.02 g/mol — guide the selection of appropriate sample preparation and analytical techniques. Nitrogen-containing functional groups confer excellent ionization efficiency in positive-ion electrospray (ESI) mode, making the compound well suited to LC-MS/MS analysis.

This reference standard is suitable for quantitative analysis on major chromatographic platforms including HPLC, GC, LC-MS/MS, and GC-MS, serving as an external calibration standard or a system suitability test reference material.

Physical & Chemical Properties

Molecular FormulaC7H4FIN2
Molecular Weight262.02 g/mol
AppearanceOff-white to pale yellow crystalline powder. (slight halide-like odor, faint amine-like odor, low volatility)
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)6.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1993
Halogen ContentF/I-containing
Nitrogen Atoms2

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