2-(2,6-Difluoro-4-(trifluoromethyl)phenoxy)-5-iodoaniline CAS 2244086-23-3

Purity 97%+In StockPharmaceutical Standards
CAS No.2244086-23-3
Molecular FormulaC13H7F5INO
Molecular Weight415.10 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2-(2,6-Difluoro-4-(trifluoromethyl)phenoxy)-5-iodoaniline CAS 2244086-23-3 chemical structure

Description

CATO supplies 2-(2,6-Difluoro-4-(trifluoromethyl)phenoxy)-5-iodoaniline (CAS 2244086-23-3), a certified reference material (molecular formula C13H7F5INO, MW 415.10 g/mol) for analytical method development and quality control.

Structurally, 2-(2,6-Difluoro-4-(trifluoromethyl)phenoxy)-5-iodoaniline (C13H7F5INO) contains a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage, fluorine/iodine substitution. The molecule exhibits a degree of unsaturation (DBE) of 8.0, corresponding to approximately 8 ring(s) or double-bond equivalent(s). With a molecular weight of 415.10 g/mol, it falls into the moderately-high-molecular-weight range. The high carbon-to-hydrogen ratio imparts good lipophilicity, allowing liquid-liquid extraction with non-polar solvents such as n-hexane or ethyl acetate.

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), 2-(2,6-Difluoro-4-(trifluoromethyl)phenoxy)-5-iodoaniline 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 FormulaC13H7F5INO
Molecular Weight415.10 g/mol
AppearancePale yellow to yellow crystalline powder. (slight halide-like odor, low volatility)
Purity97%+
StorageStore at room temperature, protect from light
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)8.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1998
Halogen ContentF/I-containing
Nitrogen Atoms1

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