methyl 5-iodothiophene-2-carboxylate CAS 88105-22-0

Purity 97%+In StockPharmaceutical Standards
CAS No.88105-22-0
Molecular FormulaC6H9IO2S
Molecular Weight272.10 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

methyl 5-iodothiophene-2-carboxylate CAS 88105-22-0 chemical structure

Description

As a certified reference material (CRM), methyl 5-iodothiophene-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.

CATO supplies methyl 5-iodothiophene-2-carboxylate (CAS 88105-22-0), a certified reference material (molecular formula C6H9IO2S, MW 272.10 g/mol) for analytical method development and quality control.

Structurally, methyl 5-iodothiophene-2-carboxylate (C6H9IO2S) contains a sulfone group, a carboxylic acid group, a hydroxyl group, an ether linkage, iodine substitution. The molecule exhibits a degree of unsaturation (DBE) of 2.0, corresponding to approximately 2 ring(s) or double-bond equivalent(s). With a molecular weight of 272.10 g/mol, it falls into the medium-molecular-weight range. 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 FormulaC6H9IO2S
Molecular Weight272.10 g/mol
Purity97%+
StorageStore at room temperature, keep tightly closed to prevent evaporation
Solubility (reference)Soluble in methanol, acetonitrile, DMSO, water (slightly soluble)
StabilityContains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)2.0
CAS Registry Year (est.)1982
Halogen ContentI-containing
Sulfur Atoms1

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