Methyl (Z)-3-(naphthalen-2-yl)but-2-enoate CAS 565190-67-2

Purity 97%+In StockPharmaceutical Standards
CAS No.565190-67-2
Molecular FormulaC15H14O2
Molecular Weight226.27 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

Methyl (Z)-3-(naphthalen-2-yl)but-2-enoate CAS 565190-67-2 chemical structure

Description

The occurrence of Methyl (Z)-3-(naphthalen-2-yl)but-2-enoate is closely related to a carboxylic acid group, a hydroxyl group, an ether linkage, a polycyclic aromatic system in its molecular formula, which determines its behaviour during synthesis, purification, or degradation.

Methyl (Z)-3-(naphthalen-2-yl)but-2-enoate (CAS 565190-67-2) is a high-purity analytical reference standard with the molecular formula C15H14O2 and a molecular weight of 226.27 g/mol.

Owing to a carboxylic acid group, a hydroxyl group, an ether linkage, a polycyclic aromatic system, Methyl (Z)-3-(naphthalen-2-yl)but-2-enoate is typically pale yellow to yellow crystalline powder. Its solid-state physicochemical attributes — including a molecular weight of 226.27 g/mol — guide the selection of appropriate sample preparation and analytical techniques. The aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

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 Methyl (Z)-3-(naphthalen-2-yl)but-2-enoate 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 FormulaC15H14O2
Molecular Weight226.27 g/mol
AppearancePale yellow to yellow crystalline powder
Purity97%+
StorageStore at 2-8°C, protect from light
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)9.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1984

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