2-[(4R,5S)-4,5-Dihydro-4,5-diphenyl-2-oxazolyl]-5-(trifluoromethyl)pyridine CAS 2635322-22-2

Purity 97%+In StockPharmaceutical Standards
CAS No.2635322-22-2
Molecular FormulaC21H15F3N2O
Molecular Weight368.35 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2-[(4R,5S)-4,5-Dihydro-4,5-diphenyl-2-oxazolyl]-5-(trifluoromethyl)pyridine CAS 2635322-22-2 chemical structure

Description

2-[(4R,5S)-4,5-Dihydro-4,5-diphenyl-2-oxazolyl]-5-(trifluoromethyl)pyridine (CAS 2635322-22-2) is a high-purity analytical reference standard with the molecular formula C21H15F3N2O and a molecular weight of 368.35 g/mol.

Structurally, 2-[(4R,5S)-4,5-Dihydro-4,5-diphenyl-2-oxazolyl]-5-(trifluoromethyl)pyridine (C21H15F3N2O) contains a steroid core, an amide group, a hydroxyl group, an ether linkage, fluorine substitution. The molecule exhibits a degree of unsaturation (DBE) of 14.0, corresponding to approximately 14 ring(s) or double-bond equivalent(s). With a molecular weight of 368.35 g/mol, it falls into the moderately-high-molecular-weight range. 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 2-[(4R,5S)-4,5-Dihydro-4,5-diphenyl-2-oxazolyl]-5-(trifluoromethyl)pyridine 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 FormulaC21H15F3N2O
Molecular Weight368.35 g/mol
AppearancePale yellow to yellow crystalline powder. (slight halide-like odor, low volatility)
Purity97%+
StorageStore at 2-8°C, protect from light
Solubility (reference)Soluble in DMSO, DMF, methanol
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)14.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)2001
Halogen ContentF-containing
Nitrogen Atoms2

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