6-(3,4-Dihydroquinolin-1(2H)-yl)-2-methylnicotinaldehyde CAS 1355219-53-2

Purity 97%+In StockPharmaceutical Standards
CAS No.1355219-53-2
Molecular FormulaC16H16N2O
Molecular Weight252.31 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

6-(3,4-Dihydroquinolin-1(2H)-yl)-2-methylnicotinaldehyde CAS 1355219-53-2 chemical structure

Description

The occurrence of 6-(3,4-Dihydroquinolin-1(2H)-yl)-2-methylnicotinaldehyde is closely related to a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage in its molecular formula, which determines its behaviour during synthesis, purification, or degradation.

6-(3,4-Dihydroquinolin-1(2H)-yl)-2-methylnicotinaldehyde (CAS 1355219-53-2), molecular formula C16H16N2O and molecular weight 252.31 g/mol, is a CATO reference standard with documented purity and traceability.

6-(3,4-Dihydroquinolin-1(2H)-yl)-2-methylnicotinaldehyde (C16H16N2O) contains a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage. Its high carbon-to-hydrogen ratio confers good lipid solubility; these physicochemical properties determine the optimal preparation and storage of its standard solutions. The aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

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), 6-(3,4-Dihydroquinolin-1(2H)-yl)-2-methylnicotinaldehyde 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 FormulaC16H16N2O
Molecular Weight252.31 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light
Solubility (reference)Soluble in DMSO, DMF, methanol
StabilityLight-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)10.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1991
Nitrogen Atoms2

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