(4R,4′R)-2,2′-(1,3-Phenylene)bis[4,5-dihydro-4-(phenylmethyl)oxazole] CAS 1315612-06-6

Purity 97%+In StockPharmaceutical Standards
CAS No.1315612-06-6
Molecular FormulaC26H24N2O2
Molecular Weight396.48 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

(4R,4′R)-2,2′-(1,3-Phenylene)bis[4,5-dihydro-4-(phenylmethyl)oxazole] CAS 1315612-06-6 chemical structure

Description

CATO supplies (4R,4′R)-2,2′-(1,3-Phenylene)bis[4,5-dihydro-4-(phenylmethyl)oxazole] (CAS 1315612-06-6), a certified reference material (molecular formula C26H24N2O2, MW 396.48 g/mol) for analytical method development and quality control.

(4R,4′R)-2,2′-(1,3-Phenylene)bis[4,5-dihydro-4-(phenylmethyl)oxazole] (C26H24N2O2) contains a steroid core, an amide group, a hydroxyl group, an ether linkage. It is notably hygroscopic, its high carbon-to-hydrogen ratio confers good lipid solubility, the carboxyl group imparts weak acidity; 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), (4R,4′R)-2,2′-(1,3-Phenylene)bis[4,5-dihydro-4-(phenylmethyl)oxazole] 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 FormulaC26H24N2O2
Molecular Weight396.48 g/mol
AppearancePale yellow to yellow crystalline powder
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
Degree of Unsaturation (DBE)16.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1990
Nitrogen Atoms2

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