5-Iodo-6-methoxy-3,4-dihydronaphthalen-1(2H)-one CAS 436091-93-9

Purity 97%+In StockPharmaceutical Standards
CAS No.436091-93-9
Molecular FormulaC11H11IO2
Molecular Weight302.11 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

5-Iodo-6-methoxy-3,4-dihydronaphthalen-1(2H)-one CAS 436091-93-9 chemical structure

Description

CATO manufactures 5-Iodo-6-methoxy-3,4-dihydronaphthalen-1(2H)-one 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.

5-Iodo-6-methoxy-3,4-dihydronaphthalen-1(2H)-one (CAS 436091-93-9), molecular formula C11H11IO2 and molecular weight 302.11 g/mol, is a CATO reference standard with documented purity and traceability.

Structurally, 5-Iodo-6-methoxy-3,4-dihydronaphthalen-1(2H)-one (C11H11IO2) contains a carboxylic acid group, a hydroxyl group, an ether linkage, iodine substitution, an aromatic ring system. The molecule exhibits a degree of unsaturation (DBE) of 6.0, corresponding to approximately 6 ring(s) or double-bond equivalent(s). With a molecular weight of 302.11 g/mol, it falls into the moderately-high-molecular-weight range. The high carbon-to-hydrogen ratio imparts good lipophilicity, allowing liquid-liquid extraction with non-polar solvents such as n-hexane or ethyl acetate.

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 FormulaC11H11IO2
Molecular Weight302.11 g/mol
AppearanceOff-white to pale 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)6.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)2025
Halogen ContentI-containing

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