2-Chloro-4-methoxy-6-(4-methoxynaphthalen-1-yl)-1,3,5-triazine CAS 65103-16-4

Purity 97%+In StockPharmaceutical Standards
CAS No.65103-16-4
Molecular FormulaC15H12ClN3O2
Molecular Weight301.73 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2-Chloro-4-methoxy-6-(4-methoxynaphthalen-1-yl)-1,3,5-triazine CAS 65103-16-4 chemical structure

Description

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

2-Chloro-4-methoxy-6-(4-methoxynaphthalen-1-yl)-1,3,5-triazine (CAS 65103-16-4), molecular formula C15H12ClN3O2 and molecular weight 301.73 g/mol, is a CATO reference standard with documented purity and traceability.

Structurally, 2-Chloro-4-methoxy-6-(4-methoxynaphthalen-1-yl)-1,3,5-triazine (C15H12ClN3O2) contains a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage, chlorine substitution. The molecule exhibits a degree of unsaturation (DBE) of 11.0, corresponding to approximately 11 ring(s) or double-bond equivalent(s). With a molecular weight of 301.73 g/mol, it falls into the moderately-high-molecular-weight range. The presence of an aromatic ring or conjugated system gives the compound characteristic absorption bands in the UV-Vis region, making it well suited to UV or diode-array detection (DAD).

CATO manufactures 2-Chloro-4-methoxy-6-(4-methoxynaphthalen-1-yl)-1,3,5-triazine 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 FormulaC15H12ClN3O2
Molecular Weight301.73 g/mol
AppearancePale yellow to yellow crystalline powder. (slight halide-like odor)
Purity97%+
StorageStore at 2-8°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)11.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1975
Halogen ContentCl-containing
Nitrogen Atoms3

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