N-Carbamimidoyl-3-(methylsulfonyl)-4-(piperidin-1-yl)benzamide CAS 141923-47-9

Purity 97%+In StockPharmaceutical Standards
CAS No.141923-47-9
Molecular FormulaC14H20N4O3S
Molecular WeightN/A
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

N-Carbamimidoyl-3-(methylsulfonyl)-4-(piperidin-1-yl)benzamide CAS 141923-47-9 chemical structure

Description

N-Carbamimidoyl-3-(methylsulfonyl)-4-(piperidin-1-yl)benzamide (CAS 141923-47-9) is a high-purity analytical reference standard with the molecular formula C14H20N4O3SHCl and a molecular weight of 360.86 g/mol.

Structurally, N-Carbamimidoyl-3-(methylsulfonyl)-4-(piperidin-1-yl)benzamide (C14H20N4O3SHCl) contains a nitrogen-containing heterocyclic scaffold, an amide group, a sulfone group, a hydroxyl group, an ether linkage, chlorine substitution. The molecule exhibits a degree of unsaturation (DBE) of 6.0, corresponding to approximately 6 ring(s) or double-bond equivalent(s). With a molecular weight of 360.86 g/mol, it falls into the moderately-high-molecular-weight range. 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).

This reference standard is suitable for quantitative analysis on major chromatographic platforms including HPLC, GC, LC-MS/MS, and GC-MS, serving as an external calibration standard or a system suitability test reference material.

As a certified reference material (CRM), N-Carbamimidoyl-3-(methylsulfonyl)-4-(piperidin-1-yl)benzamide 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 FormulaC14H20N4O3S HCl
Molecular Weight360.86 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)6.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1997
Halogen ContentCl-containing
Nitrogen Atoms4
Sulfur Atoms1

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