Methy 3-iodo-1H-indole-2-carboxylate CAS 534595-85-2

Purity 97%+In StockPharmaceutical Standards
CAS No.534595-85-2
Molecular FormulaC10H8INO2
Molecular Weight301.08 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

Methy 3-iodo-1H-indole-2-carboxylate CAS 534595-85-2 chemical structure

Description

Compared with other compounds in its class, the molecular weight of 301.08 g/mol gives Methy 3-iodo-1H-indole-2-carboxylate distinctive chromatographic separation conditions and mass-spectrometry parameter settings.

CATO supplies Methy 3-iodo-1H-indole-2-carboxylate (CAS 534595-85-2), a certified reference material (molecular formula C10H8INO2, MW 301.08 g/mol) for analytical method development and quality control.

Owing to a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage, iodine substitution, Methy 3-iodo-1H-indole-2-carboxylate is typically off-white to pale yellow crystalline powder. Its solid-state physicochemical attributes — including a molecular weight of 301.08 g/mol — guide the selection of appropriate sample preparation and analytical techniques. 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.

CATO manufactures Methy 3-iodo-1H-indole-2-carboxylate 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 FormulaC10H8INO2
Molecular Weight301.08 g/mol
AppearanceOff-white to pale yellow crystalline powder. (slight halide-like odor, faint amine-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)7.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1984
Halogen ContentI-containing
Nitrogen Atoms1

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