6-Bromo-3-(1,2,3,6-tetrahydropyridin-4-yl)-1H-indole CAS 1247577-87-2

Purity 97%+In StockPharmaceutical Standards
CAS No.1247577-87-2
Molecular FormulaC13H13BrN2
Molecular Weight277.16 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

6-Bromo-3-(1,2,3,6-tetrahydropyridin-4-yl)-1H-indole CAS 1247577-87-2 chemical structure

Description

Owing to a nitrogen-containing heterocyclic scaffold, a nitrile group, bromine substitution, 6-Bromo-3-(1,2,3,6-tetrahydropyridin-4-yl)-1H-indole is typically pale yellow to yellow low-melting solid. Its solid-state physicochemical attributes — including a molecular weight of 277.16 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.

CATO supplies 6-Bromo-3-(1,2,3,6-tetrahydropyridin-4-yl)-1H-indole (CAS 1247577-87-2), a certified reference material (molecular formula C13H13BrN2, MW 277.16 g/mol) for analytical method development and quality control.

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.

As a certified reference material (CRM), 6-Bromo-3-(1,2,3,6-tetrahydropyridin-4-yl)-1H-indole 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 FormulaC13H13BrN2
Molecular Weight277.16 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)8.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1990
Halogen ContentBr-containing
Nitrogen Atoms2

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