N-(1,2,3,4-Tetrahydronaphthalen-1-yl)cyclopentanecarboxamide CAS 794557-15-6

Purity 97%+In StockPharmaceutical Standards
CAS No.794557-15-6
Molecular FormulaC16H21NO
Molecular Weight243.34 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

N-(1,2,3,4-Tetrahydronaphthalen-1-yl)cyclopentanecarboxamide CAS 794557-15-6 chemical structure

Description

Compared with other compounds in its class, the molecular weight of 243.34 g/mol gives N-(1,2,3,4-Tetrahydronaphthalen-1-yl)cyclopentanecarboxamide distinctive chromatographic separation conditions and mass-spectrometry parameter settings.

CATO supplies N-(1,2,3,4-Tetrahydronaphthalen-1-yl)cyclopentanecarboxamide (CAS 794557-15-6), a certified reference material (molecular formula C16H21NO, MW 243.34 g/mol) for analytical method development and quality control.

The molecular framework of N-(1,2,3,4-Tetrahydronaphthalen-1-yl)cyclopentanecarboxamide (C16H21NO) is characterized by a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage. 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 N-(1,2,3,4-Tetrahydronaphthalen-1-yl)cyclopentanecarboxamide 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 FormulaC16H21NO
Molecular Weight243.34 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
StabilityLight-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)7.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1986
Nitrogen Atoms1

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