5-(Trifluoromethyl)-1,2,3,4-tetrahydronaphthalene CAS 1204295-76-0

Purity 97%+In StockPharmaceutical Standards
CAS No.1204295-76-0
Molecular FormulaC11H11F3
Molecular Weight200.20 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

5-(Trifluoromethyl)-1,2,3,4-tetrahydronaphthalene CAS 1204295-76-0 chemical structure

Description

The occurrence of 5-(Trifluoromethyl)-1,2,3,4-tetrahydronaphthalene is closely related to fluorine substitution, an aromatic ring system in its molecular formula, which determines its behaviour during synthesis, purification, or degradation.

CATO supplies 5-(Trifluoromethyl)-1,2,3,4-tetrahydronaphthalene (CAS 1204295-76-0), a certified reference material (molecular formula C11H11F3, MW 200.20 g/mol) for analytical method development and quality control.

The molecular framework of 5-(Trifluoromethyl)-1,2,3,4-tetrahydronaphthalene (C11H11F3) is characterized by fluorine substitution, an aromatic ring system. 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 high carbon-to-hydrogen ratio imparts good lipophilicity, allowing liquid-liquid extraction with non-polar solvents such as n-hexane or ethyl acetate.

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 5-(Trifluoromethyl)-1,2,3,4-tetrahydronaphthalene 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 FormulaC11H11F3
Molecular Weight200.20 g/mol
Purity97%+
StorageStore at room temperature, keep tightly closed to prevent evaporation
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate
StabilityMay oxidize slowly on prolonged air exposure
Degree of Unsaturation (DBE)5.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1990
Halogen ContentF-containing

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