n-(Furan-2-ylmethyl)-4-iodobenzamide CAS 329209-85-0

Purity 97%+In StockPharmaceutical Standards
CAS No.329209-85-0
Molecular FormulaC12H10INO2
Molecular Weight327.12 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

n-(Furan-2-ylmethyl)-4-iodobenzamide CAS 329209-85-0 chemical structure

Description

The occurrence of n-(Furan-2-ylmethyl)-4-iodobenzamide is closely related to a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage, iodine substitution in its molecular formula, which determines its behaviour during synthesis, purification, or degradation.

CATO supplies n-(Furan-2-ylmethyl)-4-iodobenzamide (CAS 329209-85-0), a certified reference material (molecular formula C12H10INO2, MW 327.12 g/mol) for analytical method development and quality control.

Structurally, n-(Furan-2-ylmethyl)-4-iodobenzamide (C12H10INO2) contains a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage, 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 327.12 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).

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), n-(Furan-2-ylmethyl)-4-iodobenzamide 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 FormulaC12H10INO2
Molecular Weight327.12 g/mol
AppearancePale yellow to yellow crystalline powder. (slight halide-like odor)
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)8.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)2025
Halogen ContentI-containing
Nitrogen Atoms1

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