1-Boc-4-iodo-2,3-dihydro-1H-indole CAS 954239-31-7

Purity 97%+In StockPharmaceutical Standards
CAS No.954239-31-7
Molecular FormulaC13H16INO2
Molecular Weight345.18 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

1-Boc-4-iodo-2,3-dihydro-1H-indole CAS 954239-31-7 chemical structure

Description

Compared with other compounds in its class, the molecular weight of 345.18 g/mol gives 1-Boc-4-iodo-2,3-dihydro-1H-indole distinctive chromatographic separation conditions and mass-spectrometry parameter settings.

1-Boc-4-iodo-2,3-dihydro-1H-indole (CAS 954239-31-7) is a high-purity analytical reference standard with the molecular formula C13H16INO2 and a molecular weight of 345.18 g/mol.

1-Boc-4-iodo-2,3-dihydro-1H-indole (C13H16INO2) contains a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage, iodine substitution. Halogen substitution raises its density and boiling point, its high carbon-to-hydrogen ratio confers good lipid solubility, the carboxyl group imparts weak acidity; these physicochemical properties determine the optimal preparation and storage of its standard solutions. 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.

CATO manufactures 1-Boc-4-iodo-2,3-dihydro-1H-indole 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.

Physical & Chemical Properties

Molecular FormulaC13H16INO2
Molecular Weight345.18 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.)1987
Halogen ContentI-containing
Nitrogen Atoms1

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