Methyl 3-bromo-4,5,6,7-tetrahydrobenzo[c]thiophene-1-carboxylate CAS 188240-62-2

Purity 97%+In StockPharmaceutical Standards
CAS No.188240-62-2
Molecular FormulaC10H11BrO2S
Molecular Weight275.16 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

Methyl 3-bromo-4,5,6,7-tetrahydrobenzo[c]thiophene-1-carboxylate CAS 188240-62-2 chemical structure

Description

As a certified reference material (CRM), Methyl 3-bromo-4,5,6,7-tetrahydrobenzo[c]thiophene-1-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 3-bromo-4,5,6,7-tetrahydrobenzo[c]thiophene-1-carboxylate (CAS 188240-62-2), a certified reference material (molecular formula C10H11BrO2S, MW 275.16 g/mol) for analytical method development and quality control.

Methyl 3-bromo-4,5,6,7-tetrahydrobenzo[c]thiophene-1-carboxylate (C10H11BrO2S) contains a sulfone group, a carboxylic acid group, a hydroxyl group, an ether linkage, bromine substitution, an aromatic ring system. 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 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 FormulaC10H11BrO2S
Molecular Weight275.16 g/mol
Purity97%+
StorageStore at room temperature, keep tightly closed to prevent evaporation
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
StabilityMay oxidize slowly on prolonged air exposure; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)5.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)2010
Halogen ContentBr-containing
Sulfur Atoms1

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