4-(2-Fluorophenyl)-N-(4-nitrophenyl)piperazine-1-carbothioamide CAS 756491-67-5

Purity 97%+In StockPharmaceutical Standards
CAS No.756491-67-5
Molecular FormulaC17H17FN4O2S
Molecular Weight360.41 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

4-(2-Fluorophenyl)-N-(4-nitrophenyl)piperazine-1-carbothioamide CAS 756491-67-5 chemical structure

Description

CATO supplies 4-(2-Fluorophenyl)-N-(4-nitrophenyl)piperazine-1-carbothioamide (CAS 756491-67-5), a certified reference material (molecular formula C17H17FN4O2S, MW 360.41 g/mol) for analytical method development and quality control.

Structurally, 4-(2-Fluorophenyl)-N-(4-nitrophenyl)piperazine-1-carbothioamide (C17H17FN4O2S) contains a steroid core, an amide group, a sulfone group, a hydroxyl group, an ether linkage, fluorine substitution. The molecule exhibits a degree of unsaturation (DBE) of 11.0, corresponding to approximately 11 ring(s) or double-bond equivalent(s). With a molecular weight of 360.41 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 4-(2-Fluorophenyl)-N-(4-nitrophenyl)piperazine-1-carbothioamide 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 FormulaC17H17FN4O2S
Molecular Weight360.41 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)11.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1986
Halogen ContentF-containing
Nitrogen Atoms4
Sulfur Atoms1

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