(2E)-3-(2-Iodophenyl)prop-2-enoic acid CAS 90276-19-0

Purity 97%+In StockPharmaceutical Standards
CAS No.90276-19-0
Molecular FormulaC9H7IO2
Molecular Weight274.06 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

(2E)-3-(2-Iodophenyl)prop-2-enoic acid CAS 90276-19-0 chemical structure

Description

Recommended for analytical method development and validation; each product is supplied with a full Certificate of Analysis (COA) ensuring ISO 17034 metrological traceability.

(2E)-3-(2-Iodophenyl)prop-2-enoic acid (CAS 90276-19-0) is a high-purity analytical reference standard with the molecular formula C9H7IO2 and a molecular weight of 274.06 g/mol.

The molecular framework of (2E)-3-(2-Iodophenyl)prop-2-enoic acid (C9H7IO2) is characterized by a carboxylic acid group, a hydroxyl group, an ether linkage, iodine substitution, an aromatic ring system. In reversed-phase chromatography, its retention is governed primarily by the polarity and ionization state of its functional groups, which provides a practical basis for HPLC-UV/DAD or LC-MS method development. 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).

CATO manufactures (2E)-3-(2-Iodophenyl)prop-2-enoic acid 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 FormulaC9H7IO2
Molecular Weight274.06 g/mol
AppearanceOff-white to pale yellow crystalline powder. (slight halide-like odor)
Purity97%+
StorageStore at 2-8°C, protect from light, keep tightly closed to prevent evaporation
Solubility (reference)Soluble in methanol, acetonitrile, DMSO, water (slightly soluble)
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.)1982
Halogen ContentI-containing

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