6-(3,6-Dihydro-2H-pyran-4-yl)-1H-indole CAS 885273-45-0

Purity 97%+In StockPharmaceutical Standards
CAS No.885273-45-0
Molecular FormulaC13H13NO
Molecular Weight199.25 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

6-(3,6-Dihydro-2H-pyran-4-yl)-1H-indole CAS 885273-45-0 chemical structure

Description

Compared with other compounds in its class, the molecular weight of 199.25 g/mol gives 6-(3,6-Dihydro-2H-pyran-4-yl)-1H-indole distinctive chromatographic separation conditions and mass-spectrometry parameter settings.

6-(3,6-Dihydro-2H-pyran-4-yl)-1H-indole (CAS 885273-45-0), molecular formula C13H13NO and molecular weight 199.25 g/mol, is a CATO reference standard with documented purity and traceability.

The molecular framework of 6-(3,6-Dihydro-2H-pyran-4-yl)-1H-indole (C13H13NO) 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. Nitrogen-containing functional groups confer excellent ionization efficiency in positive-ion electrospray (ESI) mode, making the compound well suited to LC-MS/MS analysis.

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 6-(3,6-Dihydro-2H-pyran-4-yl)-1H-indole 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 FormulaC13H13NO
Molecular Weight199.25 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)8.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1987
Nitrogen Atoms1

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