N-(2-chlorobenzyl)thiazolidine-4-carboxamide hydrochloride CAS 1587457-59-7

Purity 97%+In StockPharmaceutical Standards
CAS No.1587457-59-7
Molecular FormulaC11H13ClN2OS
Molecular WeightN/A
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

N-(2-chlorobenzyl)thiazolidine-4-carboxamide hydrochloride CAS 1587457-59-7 chemical structure

Description

Based on its molecular formula C11H13ClN2OSHCl, N-(2-chlorobenzyl)thiazolidine-4-carboxamide hydrochloride contains a nitrogen-containing heterocyclic scaffold, an amide group, sulfur-containing functionality, a hydroxyl group, an ether linkage, chlorine substitution; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 293.21 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. The high carbon-to-hydrogen ratio imparts good lipophilicity, allowing liquid-liquid extraction with non-polar solvents such as n-hexane or ethyl acetate.

N-(2-chlorobenzyl)thiazolidine-4-carboxamide hydrochloride (CAS 1587457-59-7), molecular formula C11H13ClN2OSHCl and molecular weight 293.21 g/mol, is a CATO reference standard with documented purity and traceability.

Recommended for analytical method development and validation; each product is supplied with a full Certificate of Analysis (COA) ensuring ISO 17034 metrological traceability.

CATO manufactures N-(2-chlorobenzyl)thiazolidine-4-carboxamide hydrochloride under ISO 17034:2016 accreditation with dual CNAS and ANAB accreditation. Each batch is characterized by orthogonal methods and supplied with a full Certificate of Analysis (COA), ensuring metrological traceability.

Physical & Chemical Properties

Molecular FormulaC11H13ClN2OS HCl
Molecular Weight293.21 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)5.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1993
Halogen ContentCl-containing
Nitrogen Atoms2
Sulfur Atoms1

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