Ethyl 6-iodo-4H-thieno[3,2-b]pyrrole-2-carboxylate CAS 2820190-46-1

Purity 97%+In StockPharmaceutical Standards
CAS No.2820190-46-1
Molecular FormulaC9H8INO2S
Molecular Weight321.13 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

Ethyl 6-iodo-4H-thieno[3,2-b]pyrrole-2-carboxylate CAS 2820190-46-1 chemical structure

Description

Structurally, Ethyl 6-iodo-4H-thieno[3,2-b]pyrrole-2-carboxylate (C9H8INO2S) contains a nitrogen-containing heterocyclic scaffold, an amide group, a sulfone group, a hydroxyl group, an ether linkage, iodine substitution. 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 321.13 g/mol, it falls into the moderately-high-molecular-weight range. 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).

Ethyl 6-iodo-4H-thieno[3,2-b]pyrrole-2-carboxylate (CAS 2820190-46-1), molecular formula C9H8INO2S and molecular weight 321.13 g/mol, is a CATO reference standard with documented purity and traceability.

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

As a certified reference material (CRM), Ethyl 6-iodo-4H-thieno[3,2-b]pyrrole-2-carboxylate meets the metrological traceability requirements of ISO/IEC 17025 laboratories. Batch-to-batch consistency is monitored via control charts to guarantee comparable assigned values across lots.

Physical & Chemical Properties

Molecular FormulaC9H8INO2S
Molecular Weight321.13 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light
Solubility (reference)Soluble in methanol, acetonitrile, DMSO, water (slightly soluble)
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.)2003
Halogen ContentI-containing
Nitrogen Atoms1
Sulfur Atoms1

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