N-Cyclooctyl-3-((4-phenylpiperazin-1-yl)sulfonyl)thiophene-2-carboxamide CAS 1040671-52-0

Purity 97%+In StockPharmaceutical Standards
CAS No.1040671-52-0
Molecular FormulaC23H31N3O3S2
Molecular Weight461.64 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

N-Cyclooctyl-3-((4-phenylpiperazin-1-yl)sulfonyl)thiophene-2-carboxamide CAS 1040671-52-0 chemical structure

Description

N-Cyclooctyl-3-((4-phenylpiperazin-1-yl)sulfonyl)thiophene-2-carboxamide (CAS 1040671-52-0), molecular formula C23H31N3O3S2 and molecular weight 461.64 g/mol, is a CATO reference standard with documented purity and traceability.

Structurally, N-Cyclooctyl-3-((4-phenylpiperazin-1-yl)sulfonyl)thiophene-2-carboxamide (C23H31N3O3S2) contains a steroid core, an amide group, a sulfone group, a hydroxyl group, an ether linkage. The molecule exhibits a degree of unsaturation (DBE) of 10.0, corresponding to approximately 10 ring(s) or double-bond equivalent(s). With a molecular weight of 461.64 g/mol, it falls into the moderately-high-molecular-weight range. Nitrogen-containing functional groups confer excellent ionization efficiency in positive-ion electrospray (ESI) mode, making the compound well suited to LC-MS/MS analysis.

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.

CATO manufactures N-Cyclooctyl-3-((4-phenylpiperazin-1-yl)sulfonyl)thiophene-2-carboxamide 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 FormulaC23H31N3O3S2
Molecular Weight461.64 g/mol
Purity97%+
StorageStore in a cool place (≤25°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
Degree of Unsaturation (DBE)10.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1988
Nitrogen Atoms3
Sulfur Atoms2

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