trans-4-((2-((1-Benzyl-1H-indol-5-yl)amino)-6-(ethylamino)pyrimidin-4-yl)amino)cyclohexanol CAS 359886-84-3

Purity 97%+In StockPharmaceutical Standards
CAS No.359886-84-3
Molecular FormulaC27H32N6O
Molecular Weight456.58 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

trans-4-((2-((1-Benzyl-1H-indol-5-yl)amino)-6-(ethylamino)pyrimidin-4-yl)amino)cyclohexanol CAS 359886-84-3 chemical structure

Description

trans-4-((2-((1-Benzyl-1H-indol-5-yl)amino)-6-(ethylamino)pyrimidin-4-yl)amino)cyclohexanol (CAS 359886-84-3) is a high-purity analytical reference standard with the molecular formula C27H32N6O and a molecular weight of 456.58 g/mol.

The molecular framework of trans-4-((2-((1-Benzyl-1H-indol-5-yl)amino)-6-(ethylamino)pyrimidin-4-yl)amino)cyclohexanol (C27H32N6O) is characterized by a steroid core, an amide group, a hydroxyl group, an ether linkage. In reversed-phase chromatography, its retention is governed primarily by the protonation state of its nitrogen-containing groups, which provides a practical basis for HPLC-UV/DAD or LC-MS method development. The aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

This reference standard is suitable for quantitative analysis on major chromatographic platforms including HPLC, GC, LC-MS/MS, and GC-MS, serving as an external calibration standard or a system suitability test reference material.

CATO manufactures trans-4-((2-((1-Benzyl-1H-indol-5-yl)amino)-6-(ethylamino)pyrimidin-4-yl)amino)cyclohexanol 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 FormulaC27H32N6O
Molecular Weight456.58 g/mol
AppearancePale yellow to yellow crystalline powder
Purity97%+
StorageStore at room temperature, protect from light
Solubility (reference)Soluble in DMSO, DMF, methanol
StabilityLight-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)15.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)2025
Nitrogen Atoms6

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