(E)-4-(3-(3,4-dichlorophenyl)-3-oxoprop-1-en-1-yl)phenyl thiophene-2-carboxylate CAS 329702-32-1

Purity 97%+In StockPharmaceutical Standards
CAS No.329702-32-1
Molecular FormulaC20H12Cl2O3S
Molecular Weight403.28 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

(E)-4-(3-(3,4-dichlorophenyl)-3-oxoprop-1-en-1-yl)phenyl thiophene-2-carboxylate CAS 329702-32-1 chemical structure

Description

(E)-4-(3-(3,4-dichlorophenyl)-3-oxoprop-1-en-1-yl)phenyl thiophene-2-carboxylate (CAS 329702-32-1) is a high-purity analytical reference standard with the molecular formula C20H12Cl2O3S and a molecular weight of 403.28 g/mol.

Based on its molecular formula C20H12Cl2O3S, (E)-4-(3-(3,4-dichlorophenyl)-3-oxoprop-1-en-1-yl)phenyl thiophene-2-carboxylate contains a steroid core, a sulfone group, a hydroxyl group, an ether linkage, chlorine substitution; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 403.28 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. The high carbon-to-hydrogen ratio imparts good lipophilicity, allowing liquid-liquid extraction with non-polar solvents such as n-hexane or ethyl acetate.

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

CATO manufactures (E)-4-(3-(3,4-dichlorophenyl)-3-oxoprop-1-en-1-yl)phenyl thiophene-2-carboxylate 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 FormulaC20H12Cl2O3S
Molecular Weight403.28 g/mol
Purity97%+
StorageStore at room temperature, protect from light, keep sealed and dry
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)14.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)2025
Halogen ContentCl-containing
Sulfur Atoms1

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