1-((4-Bromophenyl)sulfonyl)-3-iodo-1H-pyrrolo[2,3-c]pyridine CAS 1638772-30-1

Purity 97%+In StockPharmaceutical Standards
CAS No.1638772-30-1
Molecular FormulaC13H8BrIN2O2S
Molecular Weight463.09 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

1-((4-Bromophenyl)sulfonyl)-3-iodo-1H-pyrrolo[2,3-c]pyridine CAS 1638772-30-1 chemical structure

Description

1-((4-Bromophenyl)sulfonyl)-3-iodo-1H-pyrrolo[2,3-c]pyridine (CAS 1638772-30-1), molecular formula C13H8BrIN2O2S and molecular weight 463.09 g/mol, is a CATO reference standard with documented purity and traceability.

Structurally, 1-((4-Bromophenyl)sulfonyl)-3-iodo-1H-pyrrolo[2,3-c]pyridine (C13H8BrIN2O2S) contains a nitrogen-containing heterocyclic scaffold, an amide group, a sulfone group, a hydroxyl group, an ether linkage, bromine/iodine substitution. The molecule exhibits a degree of unsaturation (DBE) of 10.0, corresponding to approximately 10 ring(s) or double-bond equivalent(s). With a molecular weight of 463.09 g/mol, it falls into the moderately-high-molecular-weight range. 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.

CATO manufactures 1-((4-Bromophenyl)sulfonyl)-3-iodo-1H-pyrrolo[2,3-c]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 FormulaC13H8BrIN2O2S
Molecular Weight463.09 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.)1993
Halogen ContentBr/I-containing
Nitrogen Atoms2
Sulfur Atoms1

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