(2-Iodo-5-(trifluoromethoxy)phenyl)methanol CAS 2167829-73-2

Purity 97%+In StockPharmaceutical Standards
CAS No.2167829-73-2
Molecular FormulaC8H6F3IO2
Molecular Weight318.03 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

(2-Iodo-5-(trifluoromethoxy)phenyl)methanol CAS 2167829-73-2 chemical structure

Description

(2-Iodo-5-(trifluoromethoxy)phenyl)methanol (CAS 2167829-73-2), molecular formula C8H6F3IO2 and molecular weight 318.03 g/mol, is a CATO reference standard with documented purity and traceability.

Structurally, (2-Iodo-5-(trifluoromethoxy)phenyl)methanol (C8H6F3IO2) contains a carboxylic acid group, a hydroxyl group, an ether linkage, fluorine/iodine substitution, an aromatic ring system. The molecule exhibits a degree of unsaturation (DBE) of 4.0, corresponding to approximately 4 ring(s) or double-bond equivalent(s). With a molecular weight of 318.03 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).

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-Iodo-5-(trifluoromethoxy)phenyl)methanol 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 FormulaC8H6F3IO2
Molecular Weight318.03 g/mol
AppearanceOff-white to pale yellow crystalline powder. (slight halide-like odor, low volatility)
Purity97%+
StorageStore at room temperature
Solubility (reference)Soluble in methanol, acetonitrile, DMSO, water (slightly soluble)
StabilityMay oxidize slowly on prolonged air exposure; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)4.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1998
Halogen ContentF/I-containing

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