3-(Cyclohexylmethyl)-4-(trifluoromethyl)phenol CAS 1243312-98-2

Purity 97%+In StockPharmaceutical Standards
CAS No.1243312-98-2
Molecular FormulaC14H17F3O
Molecular Weight258.28 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

3-(Cyclohexylmethyl)-4-(trifluoromethyl)phenol CAS 1243312-98-2 chemical structure

Description

The occurrence of 3-(Cyclohexylmethyl)-4-(trifluoromethyl)phenol is closely related to a hydroxyl group, an ether linkage, fluorine substitution, an aromatic ring system in its molecular formula, which determines its behaviour during synthesis, purification, or degradation.

3-(Cyclohexylmethyl)-4-(trifluoromethyl)phenol (CAS 1243312-98-2), molecular formula C14H17F3O and molecular weight 258.28 g/mol, is a CATO reference standard with documented purity and traceability.

Structurally, 3-(Cyclohexylmethyl)-4-(trifluoromethyl)phenol (C14H17F3O) contains a hydroxyl group, an ether linkage, fluorine substitution, an aromatic ring system. The molecule exhibits a degree of unsaturation (DBE) of 5.0, corresponding to approximately 5 ring(s) or double-bond equivalent(s). With a molecular weight of 258.28 g/mol, it falls into the medium-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.

The assigned purity is verified by mass-balance and quantitative NMR (qNMR) approaches, with the expanded uncertainty reported at a 95% confidence level (k=2). Batch homogeneity and stability are independently assessed for every lot.

Physical & Chemical Properties

Molecular FormulaC14H17F3O
Molecular Weight258.28 g/mol
Purity97%+
StorageStore at room temperature, keep tightly closed to prevent evaporation
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
StabilityMay oxidize slowly on prolonged air exposure
Degree of Unsaturation (DBE)5.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1990
Halogen ContentF-containing

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Why CATO?