3-fluoro-8-iodo-naphthalene-1-carboxylic acid CAS 2387595-87-9

Purity 97%+In StockPharmaceutical Standards
CAS No.2387595-87-9
Molecular FormulaC11H16FIO2
Molecular Weight326.15 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

3-fluoro-8-iodo-naphthalene-1-carboxylic acid CAS 2387595-87-9 chemical structure

Description

The occurrence of 3-fluoro-8-iodo-naphthalene-1-carboxylic acid is closely related to a carboxylic acid group, a hydroxyl group, an ether linkage, fluorine/iodine substitution in its molecular formula, which determines its behaviour during synthesis, purification, or degradation.

3-fluoro-8-iodo-naphthalene-1-carboxylic acid (CAS 2387595-87-9), molecular formula C11H16FIO2 and molecular weight 326.15 g/mol, is a CATO reference standard with documented purity and traceability.

The molecular framework of 3-fluoro-8-iodo-naphthalene-1-carboxylic acid (C11H16FIO2) is characterized by a carboxylic acid group, a hydroxyl group, an ether linkage, fluorine/iodine substitution. In reversed-phase chromatography, its retention is governed primarily by its high hydrophobicity (logP), which provides a practical basis for HPLC-UV/DAD or LC-MS method development. Halogen substitution (F/Cl/Br/I) produces a distinctive isotope pattern in mass spectrometry, a valuable aid for qualitative confirmation.

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

The assigned purity is verified by mass-balance and quantitative NMR (qNMR) approaches, with the expanded uncertainty reported at a 95% confidence level (k=2). Batch homogeneity and stability are independently assessed for every lot.

Physical & Chemical Properties

Molecular FormulaC11H16FIO2
Molecular Weight326.15 g/mol
Purity97%+
StorageStore at room temperature
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
StabilityMay oxidize slowly on prolonged air exposure; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)3.0
UV AbsorptionUV-absorbing
CAS Registry Year (est.)1999
Halogen ContentF/I-containing

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