Methyl 3-(aminomethyl)-4-fluoro-1-benzothiophene-2-carboxylate hydrochloride CAS 1305711-69-6

Purity 97%+In StockPharmaceutical Standards
CAS No.1305711-69-6
Molecular FormulaC11H10FNO2S
Molecular WeightN/A
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

Methyl 3-(aminomethyl)-4-fluoro-1-benzothiophene-2-carboxylate hydrochloride CAS 1305711-69-6 chemical structure

Description

Methyl 3-(aminomethyl)-4-fluoro-1-benzothiophene-2-carboxylate hydrochloride (CAS 1305711-69-6), molecular formula C11H10FNO2SHCl and molecular weight 275.72 g/mol, is a CATO reference standard with documented purity and traceability.

Based on its molecular formula C11H10FNO2SHCl, Methyl 3-(aminomethyl)-4-fluoro-1-benzothiophene-2-carboxylate hydrochloride contains a nitrogen-containing heterocyclic scaffold, an amide group, a sulfone group, a hydroxyl group, an ether linkage, fluorine/chlorine substitution; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 275.72 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. 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.

As a certified reference material (CRM), Methyl 3-(aminomethyl)-4-fluoro-1-benzothiophene-2-carboxylate hydrochloride 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 FormulaC11H10FNO2S HCl
Molecular Weight275.72 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light, keep tightly closed to prevent evaporation
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.)1990
Halogen ContentF/Cl-containing
Nitrogen Atoms1
Sulfur Atoms1

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