EThyl (2E)-3-(5-methylfuran-2-yl)prop-2-enoate CAS 34265-56-0

Purity 97%+In StockPharmaceutical Standards
CAS No.34265-56-0
Molecular FormulaC10H12O3
Molecular Weight180.20 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

EThyl (2E)-3-(5-methylfuran-2-yl)prop-2-enoate CAS 34265-56-0 chemical structure

Description

Under current pharmacopoeial and regulatory frameworks, quality-control requirements for this class of reference material explicitly involve the control of targets including EThyl (2E)-3-(5-methylfuran-2-yl)prop-2-enoate.

CATO supplies EThyl (2E)-3-(5-methylfuran-2-yl)prop-2-enoate (CAS 34265-56-0), a certified reference material (molecular formula C10H12O3, MW 180.20 g/mol) for analytical method development and quality control.

Structurally, EThyl (2E)-3-(5-methylfuran-2-yl)prop-2-enoate (C10H12O3) contains a carboxylic acid group, a hydroxyl group, an ether linkage, an aromatic ring system. The molecule exhibits a degree of unsaturation (DBE) of 5.0, corresponding to approximately 5 ring(s) or double-bond equivalent(s). With a molecular weight of 180.20 g/mol, it falls into the medium-molecular-weight range. 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.

The assigned purity is verified by mass-balance and quantitative NMR (qNMR) approaches, with the expanded uncertainty reported at a 95% confidence level (k=2). Batch homogeneity and stability are independently assessed for every lot.

Physical & Chemical Properties

Molecular FormulaC10H12O3
Molecular Weight180.20 g/mol
AppearanceOff-white to pale yellow crystalline powder
Purity97%+
StorageStore at 2-8°C, keep sealed and dry
Solubility (reference)Soluble in methanol, ethanol, DMSO
StabilityMay oxidize slowly on prolonged air exposure; Hygroscopic; reseal immediately after opening
Degree of Unsaturation (DBE)5.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1966

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