(3-(4-(Aminomethyl)cyclohexyl)benzo[b]thiophen-2-yl)(morpholino)methanone hydrochloride CAS 1361111-26-3

Purity 97%+In StockPharmaceutical Standards
CAS No.1361111-26-3
Molecular FormulaC20H26N2O2S
Molecular WeightN/A
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

(3-(4-(Aminomethyl)cyclohexyl)benzo[b]thiophen-2-yl)(morpholino)methanone hydrochloride CAS 1361111-26-3 chemical structure

Description

(3-(4-(Aminomethyl)cyclohexyl)benzo[b]thiophen-2-yl)(morpholino)methanone hydrochloride (C20H26N2O2SHCl) contains a steroid core, an amide group, a sulfone group, a hydroxyl group, an ether linkage, chlorine substitution. It is notably hygroscopic, 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 aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

(3-(4-(Aminomethyl)cyclohexyl)benzo[b]thiophen-2-yl)(morpholino)methanone hydrochloride (CAS 1361111-26-3) is a high-purity analytical reference standard with the molecular formula C20H26N2O2SHCl and a molecular weight of 394.96 g/mol.

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), (3-(4-(Aminomethyl)cyclohexyl)benzo[b]thiophen-2-yl)(morpholino)methanone 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 FormulaC20H26N2O2S HCl
Molecular Weight394.96 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light, keep sealed and dry
Solubility (reference)Soluble in DMSO, DMF, methanol
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light; Hygroscopic; reseal immediately after opening; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)8.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1991
Halogen ContentCl-containing
Nitrogen Atoms2
Sulfur Atoms1

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