2-(5-Fluorothiophen-2-yl)acetonitrile CAS 950604-65-6

Purity 97%+In StockPharmaceutical Standards
CAS No.950604-65-6
Molecular FormulaC6H4FNS
Molecular Weight141.17 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2-(5-Fluorothiophen-2-yl)acetonitrile CAS 950604-65-6 chemical structure

Description

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

CATO supplies 2-(5-Fluorothiophen-2-yl)acetonitrile (CAS 950604-65-6), a certified reference material (molecular formula C6H4FNS, MW 141.17 g/mol) for analytical method development and quality control.

2-(5-Fluorothiophen-2-yl)acetonitrile (C6H4FNS) contains a nitrile group, sulfur-containing functionality, fluorine substitution, an aromatic ring system. Halogen substitution raises its density and boiling point; these physicochemical properties determine the optimal preparation and storage of its standard solutions. Nitrogen-containing functional groups confer excellent ionization efficiency in positive-ion electrospray (ESI) mode, making the compound well suited to LC-MS/MS analysis.

CATO manufactures 2-(5-Fluorothiophen-2-yl)acetonitrile 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 FormulaC6H4FNS
Molecular Weight141.17 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light, keep tightly closed to prevent evaporation
Solubility (reference)Soluble in methanol, acetonitrile, DMSO
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)5.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1987
Halogen ContentF-containing
Nitrogen Atoms1
Sulfur Atoms1

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