3-(2-Iodo-4-(trifluoromethyl)phenyl)acrylic acid CAS 1262012-70-3

Purity 97%+In StockPharmaceutical Standards
CAS No.1262012-70-3
Molecular FormulaC10H6F3IO2
Molecular Weight342.05 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

3-(2-Iodo-4-(trifluoromethyl)phenyl)acrylic acid CAS 1262012-70-3 chemical structure

Description

Structurally, 3-(2-Iodo-4-(trifluoromethyl)phenyl)acrylic acid (C10H6F3IO2) 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 6.0, corresponding to approximately 6 ring(s) or double-bond equivalent(s). With a molecular weight of 342.05 g/mol, it falls into the moderately-high-molecular-weight range. The aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

3-(2-Iodo-4-(trifluoromethyl)phenyl)acrylic acid (CAS 1262012-70-3), molecular formula C10H6F3IO2 and molecular weight 342.05 g/mol, is a CATO reference standard with documented purity and traceability.

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), 3-(2-Iodo-4-(trifluoromethyl)phenyl)acrylic acid 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 FormulaC10H6F3IO2
Molecular Weight342.05 g/mol
AppearanceOff-white to pale yellow crystalline powder. (slight halide-like odor, low volatility)
Purity97%+
StorageStore at 2-8°C, 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; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)6.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1990
Halogen ContentF/I-containing

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