tert-Butyl 3,6-dibromo-9H-carbazole-9-carboxylate CAS 161992-35-4

Purity 97%+In StockPharmaceutical Standards
CAS No.161992-35-4
Molecular FormulaC17H15Br2NO2
Molecular Weight425.11 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

tert-Butyl 3,6-dibromo-9H-carbazole-9-carboxylate CAS 161992-35-4 chemical structure

Description

Owing to a steroid core, an amide group, a hydroxyl group, an ether linkage, bromine substitution, tert-Butyl 3,6-dibromo-9H-carbazole-9-carboxylate is typically pale yellow to yellow crystalline powder. Its solid-state physicochemical attributes — including a molecular weight of 425.11 g/mol — guide the selection of appropriate sample preparation and analytical techniques. The aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

tert-Butyl 3,6-dibromo-9H-carbazole-9-carboxylate (CAS 161992-35-4), molecular formula C17H15Br2NO2 and molecular weight 425.11 g/mol, is a CATO reference standard with documented purity and traceability.

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), tert-Butyl 3,6-dibromo-9H-carbazole-9-carboxylate 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 FormulaC17H15Br2NO2
Molecular Weight425.11 g/mol
AppearancePale yellow to yellow crystalline powder. (slight halide-like odor, low volatility)
Purity97%+
StorageStore at room temperature, protect from light
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light; 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.)2003
Halogen ContentBr-containing
Nitrogen Atoms1

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