1-(tert-Butyl)-2-cyclopropoxy-4-iodobenzene CAS 1243449-05-9

Purity 97%+In StockPharmaceutical Standards
CAS No.1243449-05-9
Molecular FormulaC13H17IO
Molecular Weight316.18 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

1-(tert-Butyl)-2-cyclopropoxy-4-iodobenzene CAS 1243449-05-9 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.

CATO supplies 1-(tert-Butyl)-2-cyclopropoxy-4-iodobenzene (CAS 1243449-05-9), a certified reference material (molecular formula C13H17IO, MW 316.18 g/mol) for analytical method development and quality control.

1-(tert-Butyl)-2-cyclopropoxy-4-iodobenzene (C13H17IO) contains a hydroxyl group, an ether linkage, iodine substitution, an aromatic ring system. Halogen substitution raises its density and boiling point, its high carbon-to-hydrogen ratio confers good lipid solubility; these physicochemical properties determine the optimal preparation and storage of its standard solutions. 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.

Physical & Chemical Properties

Molecular FormulaC13H17IO
Molecular Weight316.18 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
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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