2-(3-Thienyl)-1,3-dioxolane CAS 13250-82-3

Purity 97%+In StockPharmaceutical Standards
CAS No.13250-82-3
Molecular FormulaC7H8O2S
Molecular Weight156.20 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2-(3-Thienyl)-1,3-dioxolane CAS 13250-82-3 chemical structure

Description

The occurrence of 2-(3-Thienyl)-1,3-dioxolane is closely related to a sulfone group, a carboxylic acid group, a hydroxyl group, an ether linkage, an aromatic ring system in its molecular formula, which determines its behaviour during synthesis, purification, or degradation.

2-(3-Thienyl)-1,3-dioxolane (CAS 13250-82-3) is a high-purity analytical reference standard with the molecular formula C7H8O2S and a molecular weight of 156.20 g/mol.

The molecular framework of 2-(3-Thienyl)-1,3-dioxolane (C7H8O2S) is characterized by a sulfone group, a carboxylic acid group, a hydroxyl group, an ether linkage, an aromatic ring system. In reversed-phase chromatography, its retention is governed primarily by the polarity and ionization state of its functional groups, which provides a practical basis for HPLC-UV/DAD or LC-MS method development. The presence of an aromatic ring or conjugated system gives the compound characteristic absorption bands in the UV-Vis region, making it well suited to UV or diode-array detection (DAD).

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 2-(3-Thienyl)-1,3-dioxolane 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 FormulaC7H8O2S
Molecular Weight156.20 g/mol
Purity97%+
StorageStore at 2-8°C
Solubility (reference)Soluble in methanol, acetonitrile, DMSO, water (slightly soluble)
StabilityMay oxidize slowly on prolonged air exposure
Degree of Unsaturation (DBE)4.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1960
Sulfur Atoms1

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