(E)-6-phenylimidazo[2,1-b]thiazole-5-carbaldehyde O-(2,4-dichlorobenzyl) oxime CAS 338395-43-0

Purity 97%+In StockPharmaceutical Standards
CAS No.338395-43-0
Molecular FormulaC19H13Cl2N3OS
Molecular Weight402.30 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

(E)-6-phenylimidazo[2,1-b]thiazole-5-carbaldehyde O-(2,4-dichlorobenzyl) oxime CAS 338395-43-0 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.

CATO supplies (E)-6-phenylimidazo[2,1-b]thiazole-5-carbaldehyde O-(2,4-dichlorobenzyl) oxime (CAS 338395-43-0), a certified reference material (molecular formula C19H13Cl2N3OS, MW 402.30 g/mol) for analytical method development and quality control.

Structurally, (E)-6-phenylimidazo[2,1-b]thiazole-5-carbaldehyde O-(2,4-dichlorobenzyl) oxime (C19H13Cl2N3OS) contains a steroid core, an amide group, sulfur-containing functionality, a hydroxyl group, an ether linkage, chlorine substitution. The molecule exhibits a degree of unsaturation (DBE) of 14.0, corresponding to approximately 14 ring(s) or double-bond equivalent(s). With a molecular weight of 402.30 g/mol, it falls into the moderately-high-molecular-weight range. The high carbon-to-hydrogen ratio imparts good lipophilicity, allowing liquid-liquid extraction with non-polar solvents such as n-hexane or ethyl acetate.

CATO manufactures (E)-6-phenylimidazo[2,1-b]thiazole-5-carbaldehyde O-(2,4-dichlorobenzyl) 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 FormulaC19H13Cl2N3OS
Molecular Weight402.30 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)14.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)2025
Halogen ContentCl-containing
Nitrogen Atoms3
Sulfur Atoms1

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