1-Tosyl-3-(trifluoromethyl)-1H-pyrrolo[2,3-b]pyridine CAS 1027297-78-4

Purity 97%+In StockPharmaceutical Standards
CAS No.1027297-78-4
Molecular FormulaC15H11F3N2O2S
Molecular Weight340.32 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

1-Tosyl-3-(trifluoromethyl)-1H-pyrrolo[2,3-b]pyridine CAS 1027297-78-4 chemical structure

Description

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

1-Tosyl-3-(trifluoromethyl)-1H-pyrrolo[2,3-b]pyridine (CAS 1027297-78-4) is a high-purity analytical reference standard with the molecular formula C15H11F3N2O2S and a molecular weight of 340.32 g/mol.

The molecular framework of 1-Tosyl-3-(trifluoromethyl)-1H-pyrrolo[2,3-b]pyridine (C15H11F3N2O2S) is characterized by a nitrogen-containing heterocyclic scaffold, an amide group, a sulfone group, a hydroxyl group, an ether linkage, fluorine substitution. In reversed-phase chromatography, its retention is governed primarily by its high hydrophobicity (logP), which provides a practical basis for HPLC-UV/DAD or LC-MS method development. The high carbon-to-hydrogen ratio imparts good lipophilicity, allowing liquid-liquid extraction with non-polar solvents such as n-hexane or ethyl acetate.

CATO manufactures 1-Tosyl-3-(trifluoromethyl)-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.

Physical & Chemical Properties

Molecular FormulaC15H11F3N2O2S
Molecular Weight340.32 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light, keep sealed and dry
Solubility (reference)Soluble in DMSO, DMF, methanol
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light; Hygroscopic; reseal immediately after opening; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)10.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1988
Halogen ContentF-containing
Nitrogen Atoms2
Sulfur Atoms1

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