N-(3-chlorophenyl)-2-methyl-1-oxa-4-azaspiro[4.6]Undecane-4-carboxamide CAS 633299-25-9

Purity 97%+In StockPharmaceutical Standards
CAS No.633299-25-9
Molecular FormulaC17H23ClN2O2
Molecular Weight322.83 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

N-(3-chlorophenyl)-2-methyl-1-oxa-4-azaspiro[4.6]Undecane-4-carboxamide CAS 633299-25-9 chemical structure

Description

N-(3-chlorophenyl)-2-methyl-1-oxa-4-azaspiro[4.6]Undecane-4-carboxamide (CAS 633299-25-9), molecular formula C17H23ClN2O2 and molecular weight 322.83 g/mol, is a CATO reference standard with documented purity and traceability.

Owing to a steroid core, an amide group, a hydroxyl group, an ether linkage, chlorine substitution, N-(3-chlorophenyl)-2-methyl-1-oxa-4-azaspiro[4.6]Undecane-4-carboxamide is typically off-white to pale yellow crystalline powder. Its solid-state physicochemical attributes — including a molecular weight of 322.83 g/mol — guide the selection of appropriate sample preparation and analytical techniques. Halogen substitution (F/Cl/Br/I) produces a distinctive isotope pattern in mass spectrometry, a valuable aid for qualitative confirmation.

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

CATO manufactures N-(3-chlorophenyl)-2-methyl-1-oxa-4-azaspiro[4.6]Undecane-4-carboxamide 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 FormulaC17H23ClN2O2
Molecular Weight322.83 g/mol
AppearanceOff-white to pale 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)7.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1985
Halogen ContentCl-containing
Nitrogen Atoms2

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