7-Chloro-3-iodo-1-tosyl-1H-pyrrolo[2,3-c]pyridine CAS 1956364-92-3

Purity 97%+In StockPharmaceutical Standards
CAS No.1956364-92-3
Molecular FormulaC14H10ClIN2O2S
Molecular Weight432.66 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

7-Chloro-3-iodo-1-tosyl-1H-pyrrolo[2,3-c]pyridine CAS 1956364-92-3 chemical structure

Description

CATO supplies 7-Chloro-3-iodo-1-tosyl-1H-pyrrolo[2,3-c]pyridine (CAS 1956364-92-3), a certified reference material (molecular formula C14H10ClIN2O2S, MW 432.66 g/mol) for analytical method development and quality control.

Based on its molecular formula C14H10ClIN2O2S, 7-Chloro-3-iodo-1-tosyl-1H-pyrrolo[2,3-c]pyridine contains a nitrogen-containing heterocyclic scaffold, an amide group, a sulfone group, a hydroxyl group, an ether linkage, chlorine/iodine substitution; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 432.66 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. Halogen substitution (F/Cl/Br/I) produces a distinctive isotope pattern in mass spectrometry, a valuable aid for qualitative confirmation.

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

As a certified reference material (CRM), 7-Chloro-3-iodo-1-tosyl-1H-pyrrolo[2,3-c]pyridine meets the metrological traceability requirements of ISO/IEC 17025 laboratories. Batch-to-batch consistency is monitored via control charts to guarantee comparable assigned values across lots.

Physical & Chemical Properties

Molecular FormulaC14H10ClIN2O2S
Molecular Weight432.66 g/mol
Purity97%+
StorageStore in a cool place (≤25°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.)1996
Halogen ContentCl/I-containing
Nitrogen Atoms2
Sulfur Atoms1

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