N-(2-methylbenzo[d]thiazol-6-yl)pyrrolidine-3-carboxamide hydrochloride CAS 1361116-39-3

Purity 97%+In StockPharmaceutical Standards
CAS No.1361116-39-3
Molecular FormulaC13H15N3OS
Molecular WeightN/A
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

N-(2-methylbenzo[d]thiazol-6-yl)pyrrolidine-3-carboxamide hydrochloride CAS 1361116-39-3 chemical structure

Description

N-(2-methylbenzo[d]thiazol-6-yl)pyrrolidine-3-carboxamide hydrochloride (C13H15N3OSHCl) contains a nitrogen-containing heterocyclic scaffold, an amide group, sulfur-containing functionality, a hydroxyl group, an ether linkage, chlorine substitution. Halogen substitution raises its density and boiling point, its high carbon-to-hydrogen ratio confers good lipid solubility; these physicochemical properties determine the optimal preparation and storage of its standard solutions. Halogen substitution (F/Cl/Br/I) produces a distinctive isotope pattern in mass spectrometry, a valuable aid for qualitative confirmation.

CATO supplies N-(2-methylbenzo[d]thiazol-6-yl)pyrrolidine-3-carboxamide hydrochloride (CAS 1361116-39-3), a certified reference material (molecular formula C13H15N3OSHCl, MW 297.80 g/mol) for analytical method development and quality control.

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), N-(2-methylbenzo[d]thiazol-6-yl)pyrrolidine-3-carboxamide 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 FormulaC13H15N3OS HCl
Molecular Weight297.80 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light, keep tightly closed to prevent evaporation
Solubility (reference)Soluble in DMSO, DMF, methanol
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)7.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1991
Halogen ContentCl-containing
Nitrogen Atoms3
Sulfur Atoms1

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