8-Fluoro-4H-thieno[3,2-c]chromene-2-carbohydrazide CAS 351003-41-3

Purity 97%+In StockPharmaceutical Standards
CAS No.351003-41-3
Molecular FormulaC12H9FN2O2S
Molecular Weight264.28 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

8-Fluoro-4H-thieno[3,2-c]chromene-2-carbohydrazide CAS 351003-41-3 chemical structure

Description

CATO manufactures 8-Fluoro-4H-thieno[3,2-c]chromene-2-carbohydrazide 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.

CATO supplies 8-Fluoro-4H-thieno[3,2-c]chromene-2-carbohydrazide (CAS 351003-41-3), a certified reference material (molecular formula C12H9FN2O2S, MW 264.28 g/mol) for analytical method development and quality control.

The molecular framework of 8-Fluoro-4H-thieno[3,2-c]chromene-2-carbohydrazide (C12H9FN2O2S) is characterized by a nitrogen-containing heterocyclic scaffold, an amide group, a sulfone group, a hydroxyl group, an ether linkage, fluorine substitution. In reversed-phase chromatography, its retention is governed primarily by its high hydrophobicity (logP), 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.

Physical & Chemical Properties

Molecular FormulaC12H9FN2O2S
Molecular Weight264.28 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light, keep sealed and dry, keep tightly closed to prevent evaporation
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)9.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)2025
Halogen ContentF-containing
Nitrogen Atoms2
Sulfur Atoms1

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