4-(tert-Butoxy)-1-cyclopropoxy-2-iodobenzene CAS 1243356-01-5

Purity 97%+In StockPharmaceutical Standards
CAS No.1243356-01-5
Molecular FormulaC13H17IO2
Molecular Weight332.18 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

4-(tert-Butoxy)-1-cyclopropoxy-2-iodobenzene CAS 1243356-01-5 chemical structure

Description

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.

4-(tert-Butoxy)-1-cyclopropoxy-2-iodobenzene (CAS 1243356-01-5) is a high-purity analytical reference standard with the molecular formula C13H17IO2 and a molecular weight of 332.18 g/mol.

Based on its molecular formula C13H17IO2, 4-(tert-Butoxy)-1-cyclopropoxy-2-iodobenzene contains a carboxylic acid group, a hydroxyl group, an ether linkage, iodine substitution, an aromatic ring system; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 332.18 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. 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).

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

Physical & Chemical Properties

Molecular FormulaC13H17IO2
Molecular Weight332.18 g/mol
AppearanceOff-white to pale yellow crystalline powder. (slight halide-like odor)
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)5.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1990
Halogen ContentI-containing

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