(E)-2-((4-chlorobenzyl)thio)quinoline-3-carbaldehyde O-(4-(tert-butyl)benzyl) oxime CAS 692287-20-0

Purity 97%+In StockPharmaceutical Standards
CAS No.692287-20-0
Molecular FormulaC28H27ClN2OS
Molecular Weight475.04 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

(E)-2-((4-chlorobenzyl)thio)quinoline-3-carbaldehyde O-(4-(tert-butyl)benzyl) oxime CAS 692287-20-0 chemical structure

Description

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

(E)-2-((4-chlorobenzyl)thio)quinoline-3-carbaldehyde O-(4-(tert-butyl)benzyl) oxime (CAS 692287-20-0), molecular formula C28H27ClN2OS and molecular weight 475.04 g/mol, is a CATO reference standard with documented purity and traceability.

Based on its molecular formula C28H27ClN2OS, (E)-2-((4-chlorobenzyl)thio)quinoline-3-carbaldehyde O-(4-(tert-butyl)benzyl) oxime contains a steroid core, 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 475.04 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. Nitrogen-containing functional groups confer excellent ionization efficiency in positive-ion electrospray (ESI) mode, making the compound well suited to LC-MS/MS analysis.

CATO manufactures (E)-2-((4-chlorobenzyl)thio)quinoline-3-carbaldehyde O-(4-(tert-butyl)benzyl) oxime 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 FormulaC28H27ClN2OS
Molecular Weight475.04 g/mol
Purity97%+
StorageStore at room temperature, protect from light
Solubility (reference)Soluble in DMSO, DMF, methanol
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)16.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1985
Halogen ContentCl-containing
Nitrogen Atoms2
Sulfur Atoms1

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